St. Jude Medical, Atrial Fibrillation Division, Inc.Download PDFPatent Trials and Appeals BoardApr 28, 202014283818 - (D) (P.T.A.B. Apr. 28, 2020) Copy Citation UNITED STATES PATENT AND TRADEMARK OFFICE UNITED STATES DEPARTMENT OF COMMERCE United States Patent and Trademark Office Address: COMMISSIONER FOR PATENTS P.O. Box 1450 Alexandria, Virginia 22313-1450 www.uspto.gov APPLICATION NO. FILING DATE FIRST NAMED INVENTOR ATTORNEY DOCKET NO. CONFIRMATION NO. 14/283,818 05/21/2014 Jonathan L. Podmore 0E-0414USC3-82410.0554 5542 55962 7590 04/28/2020 Wiley Patent Administration 1776 K Street, NW Washington, DC 20006 EXAMINER ZINK, AMANDA L ART UNIT PAPER NUMBER 3794 NOTIFICATION DATE DELIVERY MODE 04/28/2020 ELECTRONIC Please find below and/or attached an Office communication concerning this application or proceeding. The time period for reply, if any, is set in the attached communication. Notice of the Office communication was sent electronically on above-indicated "Notification Date" to the following e-mail address(es): ASJM_Patents@abbott.com ptodocket@wiley.law PTOL-90A (Rev. 04/07) UNITED STATES PATENT AND TRADEMARK OFFICE ____________ BEFORE THE PATENT TRIAL AND APPEAL BOARD ____________ Ex parte JONATHAN L. PODMORE, GREGORY J. KAMPA, and ANDREW RADIN ____________ Appeal 2019-005540 Application 14/283,818 Technology Center 3700 ____________ Before JENNIFER D. BAHR, MICHELLE R. OSINSKI, and SEAN P. O’HANLON, Administrative Patent Judges. O’HANLON, Administrative Patent Judge. DECISION ON APPEAL STATEMENT OF THE CASE Appellant1 appeals under 35 U.S.C. § 134(a) from the Examiner’s decision to reject claims 12–21.2 We have jurisdiction over this appeal under 35 U.S.C. § 6(b). We AFFIRM. In explaining our Decision, we refer to the Specification filed May 21, 2014 (“Spec.”), the Final Office Action mailed May 31, 2018 (“Final Act.”), 1 We use the term “Appellant” to refer to “applicant” as defined in 37 C.F.R. § 1.42. Appellant identifies the real party in interest as St. Jude Medical, Atrial Fibrillation Division, Inc. Appeal Br. 2. 2 Claim 1 is canceled and claims 2–11 are withdrawn. Appeal Brief 4. Appeal 2019-005540 Application 14/283,818 2 the Appeal Brief filed December 7, 2018 (“Appeal Br.”), and the Examiner’s Answer mailed March 22, 2019 (“Ans.”). SUMMARY OF THE INVENTION Appellant’s claimed invention relates to ablation devices. Spec. ¶ 2. Claims 12 and 14 are independent. Claim 12, reproduced below from page 12 (Claims Appendix) of the Appeal Brief, is illustrative of the claimed subject matter: 12. A component for insertion into a lumen of a medical catheter, comprising: a cylindrical body including a wall that defines a plurality of lumens, the plurality of lumens comprising: a peanut shell-shaped central lumen extending along a central longitudinal axis of the cylindrical body and having a cross-sectional area; and at least two additional lumens positioned peripheral of the peanut shell-shaped central lumen, each of the at least two additional lumens having a cross- sectional area smaller than the cross-sectional area of the central lumen, and wherein the wall proximate each of the at least two additional lumens is configured to secure a pull wire thereto. REFERENCES The Examiner relies on the following prior art references in rejecting the claims on appeal: DeLaRama US 5,381,782 Jan. 17, 1995 Konstorum US 6,749,560 B1 June 15, 2004 Hyde US 7,087,064 B1 Aug. 8, 2006 Appeal 2019-005540 Application 14/283,818 3 REJECTIONS3 I. Claims 12–20 stand rejected under 35 U.S.C. § 103(a) as being unpatentable over DeLaRama and Hyde. II. Claim 21 stands rejected under 35 U.S.C. § 103(a) as being unpatentable over DeLaRama, Hyde, and Konstorum. ANALYSIS Rejection I – Obviousness based on DeLaRama and Hyde In contesting this rejection, Appellant presents arguments for independent claims 12 and 14 together and does not separately argue dependent claims 13 and 15–20. See Appeal Br. 9. We select claim 12 as representative, and claims 13–20 stand or fall with claim 12. See 37 C.F.R. § 41.37(c)(1)(iv) (2018). The Examiner finds that DeLaRama discloses a catheter component including, in relevant part, “a cylindrical body including a wall that defines a plurality of lumens (view figures 6–11) with a central lumen and multiple peripheral lumens placed on opposite sides of the central lumen (view cross- sectional views in figures 6, 8, 9 and 11).” Final Act. 5. The Examiner finds that DeLaRama “fails to explicitly disclose that the central lumen is an hourglass-shaped central lumen extending along a central longitudinal axis and having a cross-sectional area.” Id. However, the Examiner finds that “Hyde discloses a catheter device which has an hourglass shaped central lumen (view figures 7–10).” Id.; see also id. at 7 (finding that “Hyde 3 A rejection of claims 12–21 under 35 U.S.C. § 112, first paragraph, and a rejection of claims 14–21 under 35 U.S.C. § 112, second paragraph, were withdrawn by the Examiner. Ans. 6; Final Act. 3–4. Appeal 2019-005540 Application 14/283,818 4 discloses a medical catheter with a peanut shell shaped central lumen”). The Examiner determines that it would have been obvious to modify DeLaRama’s central lumen to have a peanut shell shape because it “would allow for larger and more irregularly shaped objects (such as a needle or guide) to be placed through the center of the catheter.” Id. at 6. Appellant argues “that Hyde is not a component (or member) inserted into a catheter, but rather a catheter itself.” Appeal Br. 9 (citing Final Act. 5). According to Appellant, “[a]t most, therefore, the combination of DeLaRama and Hyde results in a catheter having a peanut shell-shaped central lumen and at least two peripheral lumens.” Id. We are not persuaded by Appellant’s argument because, as discussed above, the Examiner does not rely on Hyde for teaching a component for insertion into a catheter. See Final Act. 5–6. Rather, the Examiner relies on DeLaRama as disclosing a component for insertion into a catheter including, inter alia, a cylindrical body with a central lumen. Id. at 5; see also Ans. 7–8 (explaining that DeLaRama’s component is capable of being inserted into a catheter). The Examiner relies on Hyde only for teaching a central lumen having a peanut shell shape. See Final Act. 5, 7. Thus, Appellant’s argument against Hyde individually is unpersuasive of error because the rejection is based on the combined teachings of DeLaRama and Hyde. See In re Keller, 642 F.2d 413, 426 (CCPA 1981) (“[O]ne cannot show non- obviousness by attacking references individually where, as here, the rejections are based on combinations of references.”). For the above reasons, Appellant does not apprise us of error in the Examiner’s determination that the subject matter of claim 12 would have been obvious. Accordingly, we sustain the rejection of claim 12, and of Appeal 2019-005540 Application 14/283,818 5 claims 13–20 falling therewith, as being unpatentable over DeLaRama and Hyde. Rejection II – Obviousness based on DeLaRama, Hyde, and Konstorum In contesting the rejection of claim 21, Appellant relies on the arguments presented for the independent claims. See Appeal Br. 9–10. For the reasons discussed above, Appellant’s arguments fail to apprise us of error in the rejection of the independent claims, and, likewise, fail to apprise us of error in the rejection of claim 21. Accordingly, we sustain the rejection of claim 21 as unpatentable over DeLaRama, Hyde, and Konstorum. CONCLUSION In summary, Claim(s) Rejected 35 U.S.C. § References Affirmed Reversed 12–20 103(a) DeLaRama, Hyde, 12–20 21 103(a) DeLaRama, Hyde, Konstorum 21 Overall Outcome 12–21 No time period for taking any subsequent action in connection with this appeal may be extended under 37 C.F.R. § 1.136(a). See 37 C.F.R. § 1.136(a)(1)(iv). AFFIRMED Copy with citationCopy as parenthetical citation