FDA 510(k), K022622, CEM-OSTETIC, MODELS CEMO-020O, CEMO-05P, CEMO-10P, CEMO-20P, AND CEMO-30P

FDA 510(k), K022622, CEM-OSTETIC, MODELS CEMO-020O, CEMO-05P, CEMO-10P, CEMO-20P, AND CEMO-30P

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510(K) Number: K022622
Device Name: CEM-OSTETIC, MODELS CEMO-020O, CEMO-05P, CEMO-10P, CEMO-20P, AND CEMO-30P
Manufacturer:
Device Classification Name: Filler, Bone Void, Calcium Compound
Regulation Number: 888.3045
Classification Product Code: MQV
Date Received: 08/07/2002
Decision Date: 01/09/2003
Regulation Medical Specialty: Orthopedic
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