Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Zimmer BiometLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Zimmer Trabecular Metal with 10 510(k) clearances. The most recent is a 510(k) clearance dated Sep 22, 2006: VISTA P VERTEBRAL BODY REPLACEMENT SYSTEM.
| Sep 22, 2006 | VISTA P VERTEBRAL BODY REPLACEMENT SYSTEMK061155 · MQP | 510(k) clearances |
| May 25, 2006 | TRABECULAR METAL ACETABULAR AUGMENTSK061067 · LPH | 510(k) clearances |
| Feb 27, 2006 | TRABECULAR METAL TIBIAL AND FEMORAL CONE AUGMENTSK053340 · MBH | 510(k) clearances |
| Nov 16, 2005 | THE ZIMMER TMT TRABECULAR METAL VERTEBRAL BODY REPLACEMENT SYSTEMK052950 · MQP | 510(k) clearances |
| Jul 27, 2005 | MODIFICATION TO:TRABECULAR METAL FEMORAL CONE AUGMENTS, MODELS 03-125-ZZZZK051756 · JWH | 510(k) clearances |
| May 26, 2005 | EXPLANT OSTEONECROSIS INTERVENTION IMPLANT REMOVAL SYSTEMK050766 · HWE | 510(k) clearances |
| May 11, 2005 | TRABECULAR METAL ACETABULAR REVISION SHELLSK050937 · LPH | 510(k) clearances |
| Apr 15, 2005 | THE TRABECULAR METAL BONE STABILIZATION IMPLANT, MODEL 99-11197-XX-10K050101 · HRS | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
