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FDA 510(k), K090855, EQUIVABONE OSTEOINDUCTIVE BONE GRAFT SUBSTITUTE
FDA 510(k), K090855, EQUIVABONE OSTEOINDUCTIVE BONE GRAFT SUBSTITUTE
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510(K) Number: K090855
Device Name: EQUIVABONE OSTEOINDUCTIVE BONE GRAFT SUBSTITUTE
Manufacturer: CHRISTOPHER KLACZYK
Device Classification Name: Filler, Bone Void, Calcium Compound
Regulation Number: MQV
Classification Product Code: 03/30/2009
Date Received: 09/18/2009
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
Device Name: EQUIVABONE OSTEOINDUCTIVE BONE GRAFT SUBSTITUTE
Manufacturer: CHRISTOPHER KLACZYK
Device Classification Name: Filler, Bone Void, Calcium Compound
Regulation Number: MQV
Classification Product Code: 03/30/2009
Date Received: 09/18/2009
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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