510(k) K231925

Device
MINIMA S System
Applicant
Lima Corporate S.P.A.
510(k) number
K231925
Product code
LZO
Decision
Substantially Equivalent (SESE)
Decision date
2023-07-11
Date received
2023-06-30
Regulation
888.3353
Classification name
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Kenneth Newman
Address
Via Nazionale 52 Villanova Di San Daniele Del Friuli IT 33038 33038

FDA Registration Numbers

Source Documents

510(k) summary PDF

Related GUDID Devices

Primary DIBrandCompanyPublished
08033390256070MINIMA SLIMACORPORATE SPA2023-08-30
08033390256063MINIMA SLIMACORPORATE SPA2023-08-30

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