PRIMA TT Glenoid
K-Number: K222427 · 2022-10-06
ApplicantLima Corporate S.P.A.
Decision Date2022-10-06
Product CodeMBF
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
PRIMA TT Glenoid is a medical device manufactured by Lima Corporate S.P.A.. It received FDA 510(k) clearance on 2022-10-06 under approval number K222427. The device is classified under product code MBF. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the PRIMA TT Glenoid?
PRIMA TT Glenoid is a medical device that received FDA 510(k) clearance on 2022-10-06. It is manufactured by Lima Corporate S.P.A.. The 510(k) number is K222427.
When was PRIMA TT Glenoid approved by the FDA?
PRIMA TT Glenoid received FDA 510(k) clearance on 2022-10-06, under approval number K222427.
What company makes PRIMA TT Glenoid?
PRIMA TT Glenoid is manufactured by Lima Corporate S.P.A..
What is the FDA product code for PRIMA TT Glenoid?
The FDA product code for PRIMA TT Glenoid is MBF.
Other Devices by Lima Corporate S.P.A.
Related Devices (Code: MBF)
K163397SMR Hybrid Glenoid SystemLima Corporate S.P.A.
K162068ARROW Anatomical Porous glenoidFournitures Hospitalieres Industrie
K173824Humeral Short Stem SystemShoulder Innovations, Inc.
K191963SMR Finned Short StemsLima Corporate S.P.A.
K183553Compress and Mini Compress Anti-Rotation SpindlesBiomet, Inc.
K201905SMR 140° Reverse Humeral BodyLima Corporate S.P.A.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.