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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name blade, saw, general & plastic surgery, surgical
510(k) Number K955229
Device Name WRIGHT MEDICAL TECHNOLOGY SAWBLADES
Applicant
WRIGHT MEDICAL TECHNOLOGY, INC.
5677 AIRLINE RD.
ARLINGTON,  TN  38002
Applicant Contact CRISTIE MANUEL
Correspondent
WRIGHT MEDICAL TECHNOLOGY, INC.
5677 AIRLINE RD.
ARLINGTON,  TN  38002
Correspondent Contact CRISTIE MANUEL
Regulation Number878.4820
Classification Product Code
GFA  
Date Received11/14/1995
Decision Date 01/18/1996
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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