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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Punch, Surgical
510(k) Number K874356
Device Name PIN PUNCH
Applicant
Med-Tool, Inc.
12434 Matthews Ln.
St. Louis,  MO  63127
Applicant Contact JOHN MAYERIK
Correspondent
Med-Tool, Inc.
12434 Matthews Ln.
St. Louis,  MO  63127
Correspondent Contact JOHN MAYERIK
Regulation Number878.4800
Classification Product Code
LRY  
Date Received10/23/1987
Decision Date 11/23/1987
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
Predetermined Change
Control Plan Authorized		 No
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