Synthes (Usa), LLC
Synthes (Usa), LLC holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2018.
Name variants for Synthes (Usa), LLC
as filed with FDA- Synthes (Usa), LLC
- Synthes USA, LLC
Top product codes for Synthes (Usa), LLC
Recent clearances by Synthes (Usa), LLC
- K180821 — TruMatch Graft Cage - Long Bone
- K161417 — DePuy Synthes MAXFRAME Multi-Axial Correction System
- K152239 — Zero-P Natural Plate System
- K130146 — SYNTHES SYNFLATE VERTEVRAL BALLOON SYSTEM
- K112030 — SYNTHES RADIAL HEAD PROSTHESIS SYSTEM
- K120275 — SYNTHES ACIS/VERTEBRAL SPACER CR
- K101536 — 2.7/3.5MM VA-LCP ANTERIRO CLAVICLE PLATE SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.