FDA 510(k), K032288, VITOSS SCAFFOLD FOAM BONE GRAFT MATERIAL
FDA 510(k), K032288, VITOSS SCAFFOLD FOAM BONE GRAFT MATERIAL
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510(K) Number: K032288
Device Name: VITOSS SCAFFOLD FOAM BONE GRAFT MATERIAL
Manufacturer: ORTHOVITA, INC.
Device Classification Name: filler, bone void, calcium compound
Regulation Number: 888.3045
Classification Product Code: MQV
Date Received: 07/24/2003
Decision Date: 12/19/2003
Regulation Medical Specialty: Orthopedic
Device Name: VITOSS SCAFFOLD FOAM BONE GRAFT MATERIAL
Manufacturer: ORTHOVITA, INC.
Device Classification Name: filler, bone void, calcium compound
Regulation Number: 888.3045
Classification Product Code: MQV
Date Received: 07/24/2003
Decision Date: 12/19/2003
Regulation Medical Specialty: Orthopedic
- 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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