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 |