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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Appliance, Fixation, Spinal Intervertebral Body
510(k) Number K973854
Device Name ORION ANTERIOR CERVICAL PLATE SYSTEM
Applicant
SOFAMOR DANEK USA,INC.
1800 PYRAMID PLACE
MEMPHIS,  TN  38132
Applicant Contact RICHARD W TREHARNE
Correspondent
SOFAMOR DANEK USA,INC.
1800 PYRAMID PLACE
MEMPHIS,  TN  38132
Correspondent Contact RICHARD W TREHARNE
Regulation Number888.3060
Classification Product Code
KWQ  
Date Received10/03/1997
Decision Date 03/16/1998
Decision SUBSTANTIALLY EQUIVALENT FOR SOME INDICATIONS (SN)
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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