ClearanceBrief
510(k) K060161 ยท MBP Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)

AFT ALLOGRAFT FILLER TUBE

ApplicantMusculoskeletal Transplant Foundation, Edison NJ, US
DecisionSubstantially Equivalent, Mar 21, 2006
ReceivedJan 20, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K060161

DateFirm and productCodeLinked 510(k)
Jun 16, 2016Musculoskeletal Transplant Foundation, Inc.
Musculoskeletal Transplant Foundation, AFT Diverted Tube (3/4/Filled), indicated for treatment of surgically-created osseous defects or osseous defects created from traumatic injury. It can be used in
Terminated
MBPNone listed

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