FDA 510(k), K112437, ARTHREX FRACTURE SYSTEM
FDA 510(k), K112437, ARTHREX FRACTURE SYSTEM
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510(K) Number: K112437
Device Name: ARTHREX FRACTURE SYSTEM
Manufacturer:
Device Classification Name: Washer, Bolt Nut
Regulation Number: 888.3030
Classification Product Code: HTN
Date Received: 08/24/2011
Decision Date: 12/21/2011
Regulation Medical Specialty: Orthopedic
Device Name: ARTHREX FRACTURE SYSTEM
Manufacturer:
Device Classification Name: Washer, Bolt Nut
Regulation Number: 888.3030
Classification Product Code: HTN
Date Received: 08/24/2011
Decision Date: 12/21/2011
Regulation Medical Specialty: Orthopedic