Ex Parte Zannis et alDownload PDFPatent Trial and Appeal BoardApr 11, 201311261840 (P.T.A.B. Apr. 11, 2013) Copy Citation UNITED STATES PATENT AND TRADEMARK OFFICE __________ BEFORE THE PATENT TRIAL AND APPEAL BOARD __________ Ex parte ANTHONY D. ZANNIS, PRASANNA MALAVIYA, KEITH M. MCGRATH, and HERBERT E. SCHWARTZ __________ Appeal 2011-001938 Application 11/261,840 Technology Center 3700 __________ Before ERIC GRIMES, JEFFREY N. FREDMAN, and ULRIKE W. JENKS, Administrative Patent Judges. GRIMES, Administrative Patent Judge. DECISION ON APPEAL This is an appeal under 35 U.S.C. § 134 involving claims to a surgical cannula kit. The Examiner has rejected the claims as obvious. We have jurisdiction under 35 U.S.C. § 6(b). We reverse. STATEMENT OF THE CASE The Specification discloses “cannulae and obturators that can be used to manage suture during surgery” (Spec. 1, ¶ 0002), and specifically to treat App App a def of th Figu respe claim centr prox botto the c flang from bein and h the b defin throu eal 2011-0 lication 11 ect in the e Specific res 7 and 8 ctively (id Claims 5 , reads as 5. A sur wherein al longitu imal end, t m surface annula, th e and an i the centra g open at t aving rais ody betwe wherein ing a thro gh the ent 01938 /261,840 meniscus o ation are s show per . at 7, ¶¶ 0 and 7-15 follows: gical cann the cannu dinal axis, he flange , a body ex e body inc nterior sur l opening he distal e ed threads en the ann the cannu ugh slot ex ire thickne f a knee j hown belo spective v 0021-000 are on app ula kit com la includes the cannu having a c tending fr luding a p face defin of the ann nd, the bod extending ular flang la further c tending ra ss of the f 2 oint (id. at w: iews of a c 22). eal. Claim prising a a proxima la compris entral ope om the an roximal po ing a centr ular flange y further outwardl e and the d omprises dially acro lange, the 13, ¶ 000 annula an 5, the on cannula an l end, a d ing an ann ning, a top nular flang rtion adja al axial ch to the dis including y from the istal end; a pair of sp ss the ent through sl 45). Figur d an obtur ly indepen d an obtu istal end an ular flang surface an e to the d cent to the annel exte tal end, th an exterior exterior s aced surf ire flange ot further es 7 and 8 ator, dent rator: d a e at the d a istal end o annular nding e body surface urface of aces and extending f Appeal 2011-001938 Application 11/261,840 3 distally through the proximal portion of the body from the exterior surface to the interior surface, the through slot terminating at a location distal to the bottom surface of the annular flange and proximal to the distal end of the cannula; wherein the cannula further comprises a pair of spaced surfaces defining a longitudinal slot extending through the flange, threads and body of the cannula from the proximal end to the distal end, the longitudinal slot providing a passageway between the longitudinal channel of the cannula and the exterior of the cannula along the entire length of the cannula; wherein the obturator includes a proximal portion, a distal portion terminating in a distal end, an intermediate portion and a flange between the intermediate portion and the proximal portion, the obturator being sized and shaped so that the intermediate portion is receivable and slidable in the central axial channel of the cannula; and wherein the obturator further comprises a pair of spaced surfaces defining a longitudinal slot in the distal portion, intermediate portion, flange and proximal portion. The Examiner has rejected claims 5 and 7-14 under 35 U.S.C. § 103(a) as obvious in view of Khaw,1 Bennett,2 and Reich.3 The Examiner has also rejected claim 15 as obvious in view of Khaw, Bennett, Reich and Maddocks.4 The same issue is dispositive for both of these rejections. The Examiner finds that Khaw discloses “a surgical cannula kit comprising a cannula and an obturator” (Answer 3) but that Khaw’s cannula does not include a “through slot” that terminates “at a location distal to the bottom surface of the annular flange and proximal to the distal end of the cannula,” as required by claim 5 (id. at 4-5). The Examiner finds that Bennett discloses an apparatus for surgical tissue repair that comprises “a 1 Khaw, US 2007/0276288A1, Nov. 29, 2007. 2 Bennett, US 6,491,714 B1, Dec. 10, 2002. 3 Reich et al., US 5,009,643, Apr. 23, 1991. 4 Maddocks et al., 5,211,656, May 18, 1993. Appeal 2011-001938 Application 11/261,840 4 tubular shank (cannula as claimed) … [with] a through slot (22B) for retaining free end of suture” that terminates at a location proximal to the distal end of the cannula (id. at 5). The Examiner concludes that it would have been obvious “to modify the flange of Khaw with a retaining slot in view of Bennett for providing an effective retaining or holding mechanism for the wire” (id.). The Examiner finds that Khaw and Bennett do not disclose “raised threads extending outwardly from the exterior surface of the body” (id.). The Examiner finds that Reich discloses a cannula comprising “raised threads (22) extending outwardly from the exterior surface of the body” (id.), and concludes that it would have been obvious to modify Khaw’s cannula “with raised threads extending outwardly from the exterior surface of the body … in view of Reich et al for effectively securing the cannula into tissue” (id. at 5-6). Appellants argue that “it would be completely inappropriate to put the threads from the trocar sleeve of Reich et al. onto the vascular access needle of Khaw. That would cause undue harm to the tissue being penetrated.” (Appeal Br. 4). Appellants also argue that it would not have been obvious to add a notch to Khaw’s device because “[t]here is no suture in the vascular access needle of Khaw et al. thus eliminating any incentive for adding the notch from Bennett” (id.). We agree with Appellants that the Examiner has not adequately explained why one of skill in the art would have been motivated to modify Khaw’s device to include both the notch of Bennett and the threads of Reich. Appeal 2011-001938 Application 11/261,840 5 Khaw discloses “a vascular access needle assembly to facilitate insertion of a guide wire into a subject” (Khaw 1, ¶ 0002), which “includes a sheath movable from a first position to a second position for preventing inadvertent needle sticks after use” (id. at 2, ¶ 0029). Figures 1A and 1B of Khaw are shown below: Appeal 2011-001938 Application 11/261,840 6 Figure 1A shows “a perspective view of the vascular access needle assembly … with the sheath in a first locked position, exposing the needle point” (id. at 2, ¶ 0014). Figure 1B shows a perspective view of the same needle assembly “with the sheath in a second position, the needle point covered” (id.). Khaw discloses that “[s]heath 40 can rotate and slide with respect to needle 34 to align sheath slot 42 with needle slot 36 and to cover needle point 38” (id. at 3, ¶ 0033). The vascular access needle assembly can be used to insert a guide wire into a blood vessel (id. at 1, ¶ 0009). Khaw discloses that the “vascular access needle assembly … can also be used as a biopsy needle assembly to remove body tissue to perform a biopsy” (id. at 5, ¶ 0061). Khaw discloses that, in the biopsy needle embodiment, “sheath 440 slides longitudinally along needle 434 to cover needle point 438” (id. at 5, ¶ 0065). Thus, Khaw discloses a needle assembly that can be used either to insert a guide wire into the vasculature or as a biopsy needle. The Examiner concludes that it would have been obvious to include a notch in Khaw’s needle assembly to provide a retaining mechanism for a guide wire, when the needle assembly is used as a vascular access needle (Answer 5). However, the Examiner does not dispute Appellants’ position that external threads would “cause undue harm to the tissue” (Appeal Br. 4) when the assembly was used as a vascular access needle. Therefore, the Examiner has not provided a persuasive reason for including the external, raised threads required by claim 5 in a device, like Khaw’s, that is intended for use either as a vascular access needle or as a biopsy needle. Appeal 2011-001938 Application 11/261,840 7 On the other hand, if the Examiner’s reasoning is based on modifying the device to make it a dedicated biopsy needle, the Examiner has not provided persuasive reasoning to show that it would have been obvious to add notches to the resulting threaded needle assembly. That is, the Examiner’s reason for adding a notch to Khaw’s needle assembly is to retain a guide wire, which would not be applicable to a needle assembly used as a biopsy needle. Thus, we agree with Appellants that the Examiner has not adequately explained why one of skill in the art would have modified Khaw’s needle assembly to have both the notches taught by Bennett and the threads taught by Reich on the same device. Further, the Examiner’s conclusion that it would have been obvious to include threads in Khaw’s needle assembly for use in the biopsy needle application is contrary to Khaw’s disclosure that, in the biopsy needle application, the sheath moves longitudinally with respect to the needle to cover the needle point after insertion. The Examiner has not explained how the presence of external threads would be reconciled with the longitudinal movement of Khaw’s protective sheath. Thus, we reverse the rejection of independent claim 5 and dependent claims 7-14 as being obvious in view of Khaw, Bennett and Reich. The Examiner’s rejection of claim 15 based on Khaw, Bennett, Reich and Maddocks relies on the findings and conclusions with respect to Khaw, Bennett and Reich discussed above. We therefore reverse the rejection of claim 15 for the reasons discussed above. Appeal 2011-001938 Application 11/261,840 8 SUMMARY We reverse the rejection of claims 5 and 7- 14 under 35 U.S.C. § 103(a). REVERSED lp Copy with citationCopy as parenthetical citation