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 |