FDA 510(k) Applications Submitted by Robert Zott

FDA 510(k) Number Submission Date Device Name Applicant
K090419 02/18/2009 SILS STITCH ENDOSCOPIC SUTURING DEVICE COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES
K010909 03/26/2001 NONABSORBABLE POLYPROPYLENE SURGICAL SUTURE TYCO HEALTHCARE GROUP, LP
K221013 04/05/2022 GIA Auto Suture Stapler with DST Series Technology Covidien
K111442 05/24/2011 V-LOC 180 ABSORBABLE RELOAD, V-LOC PBT NON-ABSORBABLE RELOAD, ENDO STITCH (TM) ENDOSCOPIC SUTURING DEVICE, SILS (TM)... COVIDIEN, FORMERLY US SURGICAL A DIVISON OF TYCO H
K091869 06/23/2009 SILS CLINCHER, SILS DISSECTOR, SILS GRASPER, SILS L-HOOK, SILS SHEARS COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES
K032586 08/22/2003 CAPROSYN ABSORBABLE SUTURE UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
K222641 09/01/2022 SigniaÖ Small Diameter Reloads Including Regular (Round) Tip Version Covidien
K082619 09/09/2008 SILS PORT, MODELS SILSPT5, SILSPT12 COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES
K082659 09/12/2008 MODIFIED ENDO STICH COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES
K072814 10/01/2007 CONVENIENCE KIT FOR SINGLE-INCISION LAPAROSCOPIC SURGERY AND OTHER ADVANCED LAPAROSCOPIC PROCEDURES COVIDIEN
K013671 11/06/2001 L-25 ABSORBABLE SURIGCAL SUTURE UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
K063536 11/22/2006 POLYSORB* SYNTHETIC ABSORBABLE SUTURE WITH MODIFIED PACKAGING TYCO HEALTHCARE GROUP


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