The following data is part of a premarket notification filed by Tornier, Inc. with the FDA for Aequalis Adjustable Modular Reverse Shoulder System.
Device ID | K120739 |
510k Number | K120739 |
Device Name: | AEQUALIS ADJUSTABLE MODULAR REVERSE SHOULDER SYSTEM |
Classification | Shoulder Prosthesis, Reverse Configuration |
Applicant | TORNIER, INC. 7701 FRANCE AVE SOUTH SUITE 600 Edina, MN 55435 |
Contact | Brahim Hadri |
Correspondent | Brahim Hadri TORNIER, INC. 7701 FRANCE AVE SOUTH SUITE 600 Edina, MN 55435 |
Product Code | PHX |
Subsequent Product Code | HSD |
Subsequent Product Code | KWS |
Subsequent Product Code | KWT |
CFR Regulation Number | 888.3660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-03-12 |
Decision Date | 2012-07-05 |
Summary: | summary |