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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Rod, Fixation, Intramedullary And Accessories
510(k) Number K934962
Device Name AIM SUPRACONDYLAR NAIL
Applicant
Ace Orthopedic Manufacturing Co.
14105 S. Avalon Blvd.
Los Angeles,  CA  90061
Applicant Contact CLAUDE PERING
Correspondent
Ace Orthopedic Manufacturing Co.
14105 S. Avalon Blvd.
Los Angeles,  CA  90061
Correspondent Contact CLAUDE PERING
Regulation Number888.3020
Classification Product Code
HSB  
Date Received10/18/1993
Decision Date 03/22/1994
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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