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FDA 510(k) Applications Submitted by THEKEN SURGICAL,LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K983622
10/15/1998
BODYFORM THORACO-LUMBAR FIXATION SYSTEM
THEKEN SURGICAL,LLC
K050058
01/11/2005
THEKEN REVEAL VBR SYSTEM
THEKEN SURGICAL,LLC
K012278
07/19/2001
THEKEN SMALL CEMENT RESTRICTOR
THEKEN SURGICAL,LLC
K012462
08/01/2001
THEKEN LARGE CEMENT RESTRICTOR
THEKEN SURGICAL,LLC
K010466
02/16/2001
TETHER ACFS
THEKEN SURGICAL,LLC
K032064
07/03/2003
THEKEN CPOD/LPOD VERTEBRAL BODY REPLACEMENT SYSTEM
THEKEN SURGICAL,LLC
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