FDA 510(k), K032288, VITOSS SCAFFOLD FOAM BONE GRAFT MATERIAL

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

Total pages: 660
Fully redacted pages: 517
Content pages: 143