ClearanceBrief
510(k) K071849 ยท MQV Filler, Bone Void, Calcium Compound

ALLOFUSE GEL AND PUTTY

ApplicantAllosource, Inc., Centennial CO, US
DecisionSubstantially Equivalent, Dec 4, 2008
ReceivedJul 5, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K071849

DateFirm and productCodeLinked 510(k)
May 6, 2014AlloSource, Inc.
AlloFuse DBM Putty 5cc, Catalog No. 90038005 AlloFuse is indicated for orthopedic applications as filler for gaps or voids that are not intrinsic to the stability of the bony structure. AlloFuse is i
Terminated
MQVNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.