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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 K931500
Device Name THE PERMARIDGE MATRIX CHIN
Applicant
APPLIED BIOMATERIAL TECHNOLOGIES
3500 N.W. ANDERSON HILL RD.
SUITE #101
SILVERDALE,  WA  98383
Applicant Contact GERALD HANSON
Correspondent
APPLIED BIOMATERIAL TECHNOLOGIES
3500 N.W. ANDERSON HILL RD.
SUITE #101
SILVERDALE,  WA  98383
Correspondent Contact GERALD HANSON
Regulation Number878.3550
Classification Product Code
FWP  
Date Received03/25/1993
Decision Date 11/17/1994
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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