FDA applicant
Zimmer Trabecular
FDA records 10 decisions for Zimmer Trabecular (Allendale, NJ) from 2004 to 2006: 10 510(k) clearances. Most are in product codes LPH (Prosthesis, Hip, Semi-Constrained…) and MQP (Spinal Vertebral Body Replacement Device). Its devices cite 13 predicates, 2 of them its own earlier devices. 4 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Zimmer Trabecular’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Zimmer Trabecular since 2007.
Recalls per year
4in 2010
Class I Class II/III not classified
Planning a device like Zimmer Trabecular’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”
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