The following data is part of a premarket notification filed by Tornier with the FDA for Aequalis Reversed Prosthesis.
Device ID | K061439 |
510k Number | K061439 |
Device Name: | AEQUALIS REVERSED PROSTHESIS |
Classification | Shoulder Prosthesis, Reverse Configuration |
Applicant | TORNIER 161 RUE LAVOISIER MONTBONNOT Saint-ismier Cedex, FR 38334 |
Contact | Mireille Lemery |
Correspondent | Mireille Lemery TORNIER 161 RUE LAVOISIER MONTBONNOT Saint-ismier Cedex, FR 38334 |
Product Code | PHX |
CFR Regulation Number | 888.3660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-05-24 |
Decision Date | 2006-07-20 |
Summary: | summary |