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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name screw, fixation, bone
510(k) Number K982222
Device Name SYNTHES (USA) DISTAL FEMUR PLATE (DFP) SYSTEM
Applicant
SYNTHES (USA)
P.O. BOX 1766
1690 RUSSELL ROAD
PAOLI,  PA  19301 -1222
Applicant Contact SHERI L MUSGNUNG
Correspondent
SYNTHES (USA)
P.O. BOX 1766
1690 RUSSELL ROAD
PAOLI,  PA  19301 -1222
Correspondent Contact SHERI L MUSGNUNG
Regulation Number888.3040
Classification Product Code
HWC  
Subsequent Product Codes
HRS   HTY   JDW  
Date Received06/24/1998
Decision Date 07/29/1998
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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