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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 K081700
Device Name SYNTHES (USA) STERNAL FIXATION SYSTEM - LINE EXTENSION
Applicant
Synthes (Usa)
1301 Goshen Pkwy.
19380,  PA  19380
Applicant Contact AMNON TALMOR
Correspondent
Synthes (Usa)
1301 Goshen Pkwy.
19380,  PA  19380
Correspondent Contact AMNON TALMOR
Regulation Number888.3040
Classification Product Code
HWC  
Date Received06/17/2008
Decision Date 07/17/2008
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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