Linvatec Biomaterials, Ltd. is one of 24554 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Linvatec Biomaterials, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: DUET SUTURE ANCHOR, MODELS BXS4216, BXS4216H, BIOSORB FX AND BIOSORB PDX 1.5 AND 2.0 SCREWS, SMARTSCREW II, MODELS 232010, 232012, 232014, 232016, 232018, 232020
5
Total
5
Cleared
0
Denied
Linvatec Biomaterials, Ltd. has 5 FDA 510(k) cleared medical devices. Based in Largo, US.
Historical record: 5 cleared submissions from 2003 to 2004. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Linvatec Biomaterials, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Linvatec Biomaterials, Ltd.
5 devices
Cleared
Nov 19, 2004
DUET SUTURE ANCHOR, MODELS BXS4216, BXS4216H
Orthopedic
22d
Cleared
Oct 08, 2004
BIOSORB FX AND BIOSORB PDX 1.5 AND 2.0 SCREWS
Dental
23d
Cleared
Sep 16, 2004
SMARTSCREW II, MODELS 232010, 232012, 232014, 232016, 232018, 232020
Orthopedic
23d
Cleared
Apr 16, 2004
CANNULATED NUGEN FX SCREW FULLY THREADED, CANNULATED NUGEN FX SCREW PARTIALLY...
Orthopedic
252d
Cleared
Jul 25, 2003
2.4 SMARTNAIL, MODELS 532416, 532425, 532435, 532445
Orthopedic
29d