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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Laparoscope, General & Plastic Surgery
510(k) Number K172940
Device Name ANCHOR Tissue Retrieval System
Applicant
Conmed Corporation
525 French Road
Utica,  NY  13502
Applicant Contact Rachelle D. Fitzgerald
Correspondent
Conmed Corporation
525 French Road
Utica,  NY  13502
Correspondent Contact Rachelle D. Fitzgerald
Regulation Number876.1500
Classification Product Code
GCJ  
Date Received09/26/2017
Decision Date 10/18/2017
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel General & Plastic Surgery
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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