MINIMA S System
K-Number: K231925 · 2023-07-11
ApplicantLima Corporate S.P.A.
Decision Date2023-07-11
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
MINIMA S System is a medical device manufactured by Lima Corporate S.P.A.. It received FDA 510(k) clearance on 2023-07-11 under approval number K231925. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the MINIMA S System?
MINIMA S System is a medical device that received FDA 510(k) clearance on 2023-07-11. It is manufactured by Lima Corporate S.P.A.. The 510(k) number is K231925.
When was MINIMA S System approved by the FDA?
MINIMA S System received FDA 510(k) clearance on 2023-07-11, under approval number K231925.
What company makes MINIMA S System?
MINIMA S System is manufactured by Lima Corporate S.P.A..
What is the FDA product code for MINIMA S System?
The FDA product code for MINIMA S System is LZO.
Other Devices by Lima Corporate S.P.A.
Related Devices (Code: LZO)
K160895Initia Total Hip System & BIOCERAM AZUL(R) HEADKyocera Medical Corporation
K161830Zimmer M/L Taper Hip ProsthesisZimmer, Inc.
K161192Wagner SL Revision Stem Lateral, Wagner Cone Prosthesis® SystemZimmer GmbH
K152893Corin Optimized Positioning System (OPS)Corin USA
K160289MasterLoc StemMedacta International
K152903REVIVAL(TM) Modular Revision Hip StemCorin USA
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.