510(k) K042125 ยท MQV Filler, Bone Void, Calcium Compound
AFT
| Applicant | Musculoskeletal Transplant Foundation, Edison NJ, US |
| Decision | Substantially Equivalent, Jul 28, 2005 |
| Received | Aug 6, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042125
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 9, 2024 | Musculoskeletal Transplant Foundation, Inc. AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler) Open, Classified |
MQV | None listed |
| Feb 9, 2024 | Musculoskeletal Transplant Foundation, Inc. AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bone void filler) Open, Classified |
MQV | None listed |
| Jun 16, 2016 | Musculoskeletal 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 |
MBP | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.