Vilex IN Tennessee, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories4
Latest FDA decision2019-07-29
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K191289 | Bone Screw Line Addition | HWC | 2019-07-29 | View |
| 510(k) | K190543 | Cannulated Hemi Implant | KWD | 2019-05-31 | View |
| 510(k) | K163487 | Ultima HA Coated Half Pins and Wire | JDW | 2017-02-13 | View |
| 510(k) | K151881 | X-Fix Line Additions | KTT | 2016-03-24 | View |
No matching devices.