Zimmer Trabecular Metal Technology
FDA 510(k) medical device clearances.
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.