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Variants of SMR Hybrid Glenoid System by Lima Corporate S.P.A.
2 variants
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Device · Manufacturer · Authorizations
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Status
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SMR Hybrid Glenoid System
Lima Corporate S.P.A.
·
,
FDA registration: United States
Class II
FDA 510(k)
K231099
Active
Cleared 21 Dec 2023
Active
510(k)
510(k)
II
SMR Hybrid Glenoid System
Open recall
Lima Corporate S.P.A.
·
,
FDA registration: United States
Class II
FDA 510(k)
K163397
Active
Cleared 29 Jun 2017
Active
510(k)
510(k)
II
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