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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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