FDA applicant
Zimmer Trabecular Metal Technology
FDA records 13 decisions for Zimmer Trabecular Metal Technology (Parsippany, NJ) from 2007 to 2014: 13 510(k) clearances. Most are in product codes MBH (Prosthesis, Knee, Patello/Femorotibial…) and ODP (Intervertebral Fusion Device With Bone Graft…). Its devices cite 39 predicates, 10 of them its own earlier devices. 3 recalls are linked to its devices.
FDA’s records also spell it “Zimmer Trabecular Metal Technology, Inc.”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Zimmer Trabecular Metal Technology’s devices, and how often a recall has named them.
FDA decisions per year
1in 2014
2026 so far, outlined.
Recalls per year
1in 2019
Class I Class II/III not classified
Planning a device like Zimmer Trabecular Metal Technology’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 “Zimmer”
FDA records each applicant name separately; these may or may not be the same firm.