The following data is part of a premarket notification filed by Fx Solutions with the FDA for Humeris Shoulder.
| Device ID | K163669 |
| 510k Number | K163669 |
| Device Name: | Humeris Shoulder |
| Classification | Shoulder Prosthesis, Reverse Configuration |
| Applicant | Fx Solutions 1663 Rue De Majornas Viriat, FR 01440 |
| Contact | Jean-jacques Martin |
| Correspondent | Ratsamy Thevenin Fx Solutions 1663 Rue De Majornas Viriat, FR 01440 |
| Product Code | PHX |
| Subsequent Product Code | HSD |
| Subsequent Product Code | KWT |
| CFR Regulation Number | 888.3660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-12-27 |
| Decision Date | 2017-05-17 |
| Summary: | summary |