CONCORDE LIFT
Intervertebral Fusion Device With Bone Graft, Lumbar
Medos International, SARL
The following data is part of a premarket notification filed by Medos International, Sarl with the FDA for Concorde Lift.
Pre-market Notification Details
| Device ID | K182349 |
| 510k Number | K182349 |
| Device Name: | CONCORDE LIFT |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | Medos International, SARL Chemin-Blanc 38 Le Locle, CH 2400 |
| Contact | Desiree Saracino |
| Correspondent | Desiree Saracino DePuy Synthes 325 Paramount Drive Raynham, MA 02767 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-08-29 |
| Decision Date | 2019-04-03 |
Trademark Results [CONCORDE LIFT]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CONCORDE LIFT 87235871 5509251 Live/Registered |
DePuy Synthes, Inc. 2016-11-14 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.