FDA 510(k) Applications Submitted by SPINE VISION, INC

FDA 510(k) Number Submission Date Device Name Applicant
K012881 08/28/2001 C3 ANTERIOR CERVICAL PLATE SYSTEM SPINE VISION, INC
K021507 05/09/2002 PLUS PIVOT LINK UNIVERSAL SYSTEM SPINE VISION, INC
K021510 05/09/2002 UNI-T UNI-THREAD SPINAL SYSTEM SPINE VISION, INC
K052406 09/01/2005 UNI-THREAD SPINAL SYSTEM SPINE VISION, INC


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