The following data is part of a premarket notification filed by Tornier, Inc. with the FDA for Aequalis Perform Reversed, Aequalis Perform+ Reversed Glenoid.
Device ID | K161742 |
510k Number | K161742 |
Device Name: | Aequalis PerFORM Reversed, Aequalis PerFORM+ Reversed Glenoid |
Classification | Shoulder Prosthesis, Reverse Configuration |
Applicant | Tornier, Inc. 10801 Nesbitt Avenue South Bloomington, MN 55340 |
Contact | Laurie Lewandowski |
Correspondent | Laurie Lewandowski Tornier, Inc. 10801 Nesbitt Avenue South Bloomington, MN 55340 |
Product Code | PHX |
CFR Regulation Number | 888.3660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-06-24 |
Decision Date | 2016-11-15 |
Summary: | summary |