FDA 510(k), K042899, SYNTHES (USA) RIA SYSTEM - EXPANDED INDICATIONS

FDA 510(k), K042899, SYNTHES (USA) RIA SYSTEM - EXPANDED INDICATIONS

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510(K) Number: K042899
Device Name: SYNTHES (USA) RIA SYSTEM - EXPANDED INDICATIONS
Manufacturer: SHERI L MUSGNUNG
Device Classification Name: Reamer
Regulation Number: HTO
Classification Product Code: 10/20/2004
Date Received: 03/16/2005
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
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