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26 devices found
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Manufacturer: Turnkey Intergration USA, Inc.
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Device · Manufacturer · Authorizations
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Link Endo Model Revision Cup
Turnkey Intergration USA, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K943986
Active
Cleared 5 Jul 1995
Active
510(k)
510(k)
II
Lima 28mm Ceramic Head, Modification
Turnkey Intergration USA, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K912985
Active
Cleared 24 Dec 1991
Active
510(k)
510(k)
II
Link Saddle Prothesis
Turnkey Intergration USA, Inc.
·
,
United States
(FDA 510(k) applicant)
Not classified
FDA 510(k)
K943277
Active
Cleared 26 Jan 1995
Active
510(k)
510(k)
—
Modified Freeman Acetabular Cup
Turnkey Intergration USA, Inc.
·
,
United States
(FDA 510(k) applicant)
Class III
FDA 510(k)
K902110
Active
Cleared 22 Aug 1990
Active
510(k)
510(k)
III
Link Cerclage Wire System
Turnkey Intergration USA, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K970084
Active
Cleared 13 Mar 1997
Active
510(k)
510(k)
II
Vsp Hip Stem
Turnkey Intergration USA, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K903957
Active
Cleared 26 Nov 1990
Active
510(k)
510(k)
II
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