The following data is part of a premarket notification filed by Limacorporate S.p.a. with the FDA for Prima Tt Glenoid.
| Device ID | K222427 |
| 510k Number | K222427 |
| Device Name: | PRIMA TT Glenoid |
| Classification | Prosthesis, Shoulder, Semi-constrained, Metal/polymer, Uncemented |
| Applicant | LimaCorporate S.p.A. Via Nazionale 52 Villanova Di San Daniele Del Friuli, IT 33038 |
| Contact | Michela Zanotto |
| Correspondent | Kenneth Newman Lima USA Inc. 2001 NE Green Oaks Blvd. Ste 100 Arlington, TX 76006 |
| Product Code | MBF |
| CFR Regulation Number | 888.3670 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2022-08-11 |
| Decision Date | 2022-10-06 |