The following data is part of a premarket notification filed by Stryker Orthopaedics with the FDA for Exeter V40 Femoral Stem Hip System, Orthinox V40 Femoral Heads.
Device ID | K173499 |
510k Number | K173499 |
Device Name: | Exeter V40 Femoral Stem Hip System, Orthinox V40 Femoral Heads |
Classification | Prosthesis, Hip, Femoral Component, Cemented, Metal |
Applicant | Stryker Orthopaedics 325 Corporate Drive Mahwah, NJ 07430 |
Contact | Kirsten Lehmuller |
Correspondent | Kirsten Lehmuller Stryker Orthopaedics 325 Corporate Drive Mahwah, NJ 07430 |
Product Code | JDG |
Subsequent Product Code | JDI |
Subsequent Product Code | KWY |
Subsequent Product Code | LZO |
CFR Regulation Number | 888.3360 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-11-13 |
Decision Date | 2018-03-19 |
Summary: | summary |