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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Prosthesis, Chin, Internal
510(k) Number K992239
Device Name PILLAR CHIN IMPLANT
Applicant
Pillar Surgical, Inc.
P.O. Box 8141
La Jolla,  CA  92038
Applicant Contact ROB FRITZENKOTTER
Correspondent
Pillar Surgical, Inc.
P.O. Box 8141
La Jolla,  CA  92038
Correspondent Contact ROB FRITZENKOTTER
Regulation Number878.3550
Classification Product Code
FWP  
Date Received07/02/1999
Decision Date 11/22/1999
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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