Vilex IN Tennessee, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Bone Screw Line Addition, Cannulated Hemi Implant
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Vilex IN Tennessee, Inc. Orthopedic ✕
7 devices
Cleared
Jul 29, 2019
Bone Screw Line Addition
Orthopedic
77d
Cleared
May 31, 2019
Cannulated Hemi Implant
Orthopedic
88d
Cleared
Feb 13, 2017
Ultima HA Coated Half Pins and Wire
Orthopedic
63d
Cleared
Mar 24, 2016
X-Fix Line Additions
Orthopedic
259d
Cleared
Nov 10, 2015
EzFuze Implant System
Orthopedic
284d
Cleared
Oct 29, 2015
Small Bone Nail Implant
Orthopedic
150d
Cleared
Sep 10, 2014
TRIDENT FUSION IMPLANT
Orthopedic
55d