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 |