The following data is part of a premarket notification filed by Wright Medical Technology, Inc. with the FDA for Salvation Midfoot Nail.
| Device ID | K180024 |
| 510k Number | K180024 |
| Device Name: | SALVATION Midfoot Nail |
| Classification | Screw, Fixation, Bone |
| Applicant | Wright Medical Technology, Inc. 1023 Cherry Road Memphis, TN 37117 |
| Contact | Alayne Melancon |
| Correspondent | Alayne Melancon Wright Medical Technology, Inc. 1023 Cherry Road Memphis, TN 38117 |
| Product Code | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-01-03 |
| Decision Date | 2018-07-11 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00889797070638 | K180024 | 000 |
| 00889797070515 | K180024 | 000 |
| 00889797070508 | K180024 | 000 |
| 00889797070492 | K180024 | 000 |
| 00889797070485 | K180024 | 000 |
| 00889797070478 | K180024 | 000 |
| 00889797070461 | K180024 | 000 |
| 00889797070454 | K180024 | 000 |
| 00889797070447 | K180024 | 000 |
| 00889797070522 | K180024 | 000 |
| 00889797070539 | K180024 | 000 |
| 00889797070546 | K180024 | 000 |
| 00889797070621 | K180024 | 000 |
| 00889797070614 | K180024 | 000 |
| 00889797070607 | K180024 | 000 |
| 00889797070591 | K180024 | 000 |
| 00889797070584 | K180024 | 000 |
| 00889797070577 | K180024 | 000 |
| 00889797070560 | K180024 | 000 |
| 00889797070553 | K180024 | 000 |
| 00889797070430 | K180024 | 000 |