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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Thoracolumbosacral Pedicle Screw System
510(k) Number K100634
Device Name SYNTHES MATRIX SYSTEM
Applicant
Synthes (Usa)
1302 Wrights Lane E.
West Chester,  PA  19380
Applicant Contact AMNON TALMOR
Correspondent
Synthes (Usa)
1302 Wrights Lane E.
West Chester,  PA  19380
Correspondent Contact AMNON TALMOR
Regulation Number888.3070
Classification Product Code
NKB  
Subsequent Product Codes
KWP   KWQ   MNH   MNI  
Date Received03/05/2010
Decision Date 07/01/2010
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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