The following data is part of a premarket notification filed by Synthes (usa) Products, Llc with the FDA for Depuy Synthes Femoral Recon Nail System.
| Device ID | K172157 |
| 510k Number | K172157 |
| Device Name: | DePuy Synthes Femoral Recon Nail System |
| Classification | Rod, Fixation, Intramedullary And Accessories |
| Applicant | Synthes (USA) Products, LLC 1301 Goshen Parkway West Chester, PA 19380 |
| Contact | Alexander Zwahlen |
| Correspondent | Alexander Zwahlen Synthes (USA) Products, LLC 1301 Goshen Parkway West Chester, PA 19380 |
| Product Code | HSB |
| CFR Regulation Number | 888.3020 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-07-18 |
| Decision Date | 2017-11-14 |
| Summary: | summary |