The following data is part of a premarket notification filed by Smith & Nephew with the FDA for Conquest Fn.
| Device ID | K172785 |
| 510k Number | K172785 |
| Device Name: | CONQUEST FN |
| Classification | Device, Fixation, Proximal Femoral, Implant |
| Applicant | Smith & Nephew 1450 E Brooks Road Memphis, TN 38116 |
| Contact | Allison Chan |
| Correspondent | Allison Chan Smith & Nephew 1450 E Brooks Road Memphis, TN 38116 |
| Product Code | JDO |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-09-15 |
| Decision Date | 2017-12-22 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00885556696262 | K172785 | 000 |
| 00885556696231 | K172785 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CONQUEST FN 86448071 5261497 Live/Registered |
Smith & Nephew, Inc. 2014-11-07 |