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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