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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name forceps
510(k) Number K873510
Device Name SERRATED GRASPING FORCEPS, CURVED DOWN
Applicant
ARTHROPEDICS, INC.
111 LESTER ST.
WALLINGTON,  NJ  07057
Applicant Contact JERRY PROCOPIO
Correspondent
ARTHROPEDICS, INC.
111 LESTER ST.
WALLINGTON,  NJ  07057
Correspondent Contact JERRY PROCOPIO
Regulation Number878.4800
Classification Product Code
HTD  
Date Received08/31/1987
Decision Date 11/02/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
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