Zimmer Trabecular Metal Technology
Zimmer Trabecular Metal Technology holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2014.
Top product codes for Zimmer Trabecular Metal Technology
Recent clearances by Zimmer Trabecular Metal Technology
- K133784 — VISTA-S DEVICE, ASSOCIATED INSTRUMENTATION
- K123602 — TM ARDIS INTERBODY SYSTEM INSERTER
- K120990 — NEXGEN LCCK TRABECULAR METAL (TM) COUPLED TIBIAL CONES PROVISIONALS TO NEXGEN LCCK TRABECULAR METAL (TM) COUPLED TIBIAL
- K113561 — TM ARDIS INTERBODY SYSTEM TM ARDIS INTERBODY SYSTEM INSTRUMENATION
- K111983 — VISTA-S DEVICE MODEL 08/06-401-XXXXX, 08/06-402-XXXXXX
- K103033 — TRABECULAR METAL FUSION DEVICE MODEL 06-101-XXXXX, 06-102-XXXXX AND 08-100-XXXXX
- K102896 — TRABECULAR METAL TIBIAL CONE AUGMENTS
- K093127 — TRABECULAR METAL (TM) VERTEBRAL BODY REPLACEMENT (VBR) SYSTEM INSTRUMENT SET
- K070754 — TRABECULAR METAL VERTEBRAL BODY REPLACEMENT (VBR), MODEL# 06-115, 06-155
- K071090 — TRABECULAR METAL GLENOID- B/F COMPLETE SHOULDER SOLUTION
- K070382 — VISTA -S DEVICE
Data sourced from openFDA. This site is unofficial and independent of the FDA.