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FDA 510(k) Applications Submitted by RANDY THEKEN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K050058
01/11/2005
THEKEN REVEAL VBR SYSTEM
THEKEN SURGICAL,LLC
K041592
06/14/2004
CORAL SPINAL SYSTEM
THEKEN SURGICAL
K012278
07/19/2001
THEKEN SMALL CEMENT RESTRICTOR
THEKEN SURGICAL,LLC
K012462
08/01/2001
THEKEN LARGE CEMENT RESTRICTOR
THEKEN SURGICAL,LLC
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