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 |