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 | K173537 |
| 510k Number | K173537 |
| Device Name: | CONCORDE LIFT™ |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | Medos International, SARL Chemin-Blanc 38 Le Locle, CH 2400 |
| Contact | Karen Sylvia |
| 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 | 2017-11-15 |
| Decision Date | 2018-02-08 |
| Summary: | summary |
NIH GUDID Devices
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10705034531236 | K173537 | 000 |
| 10705034507316 | K173537 | 000 |
| 10705034506944 | K173537 | 000 |
Trademark Results [CONCORDE LIFT]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CONCORDE LIFT 87235871 5509251 Live/Registered |
DePuy Synthes, Inc. 2016-11-14 |
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