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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Orthopedic Manual Surgical Instrument
510(k) Number K903247
Device Name ADJUSTABLE ANGLE GUIDE
Applicant
ONYX MEDICAL CORP.
152 COLLINS ST.
MEMPHIS,  TN  38112
Applicant Contact GEORGE W MURRAY
Correspondent
ONYX MEDICAL CORP.
152 COLLINS ST.
MEMPHIS,  TN  38112
Correspondent Contact GEORGE W MURRAY
Regulation Number888.4540
Classification Product Code
LXH  
Date Received07/24/1990
Decision Date 07/30/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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