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 |