Linvatec Biomaterials, Ltd.
Linvatec Biomaterials, Ltd. holds FDA 510(k) medical device clearances, first cleared 2003, most recent 2004.
Top product codes for Linvatec Biomaterials, Ltd.
Recent clearances by Linvatec Biomaterials, Ltd.
- K042966 — DUET SUTURE ANCHOR, MODELS BXS4216, BXS4216H; IMPACT SUTURE ANCHOR, MODELS BXS4218, BXS4218H
- K042517 — BIOSORB FX AND BIOSORB PDX 1.5 AND 2.0 SCREWS
- K042295 — SMARTSCREW II, MODELS 232010, 232012, 232014, 232016, 232018, 232020
- K032447 — CANNULATED NUGEN FX SCREW FULLY THREADED, CANNULATED NUGEN FX SCREW PARTIALLY THREADED
- K031981 — 2.4 SMARTNAIL, MODELS 532416, 532425, 532435, 532445
Data sourced from openFDA. This site is unofficial and independent of the FDA.