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 |