FDA applicant
Musculoskeletal Transplant Foundation
FDA records 24 decisions for Musculoskeletal Transplant Foundation (Edison, NJ) from 2004 to 2019: 24 510(k) clearances. Most are in product codes MQV (Filler, Bone Void, Calcium Compound) and MBP (Filler, Bone Void, Osteoinduction (W/O Human…). Its devices cite 35 predicates, 25 of them its own earlier devices. 7 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Musculoskeletal Transplant Foundation’s devices, and how often a recall has named them.
FDA decisions per year
1in 2019
2026 so far, outlined.
Recalls per year
3in 2023
Class I Class II/III not classified
Planning a device like Musculoskeletal Transplant Foundation’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Musculoskeletal”
FDA records each applicant name separately; these may or may not be the same firm.