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FDA 510(k) Applications Submitted by SPINECRAFT
FDA 510(k) Number
Submission Date
Device Name
Applicant
K090887
03/31/2009
ORIO-C CERVICAL, ORIO-TL TLIF, ORIO-PL PLIF, ORIO-AL ALIF INTERVEDRTEBRAL BODY FUSION CAGES
SPINECRAFT
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