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 |