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FDA 510(k) Applications Submitted by SPINE NEXT AMERICA CORPORATION
FDA 510(k) Number
Submission Date
Device Name
Applicant
K042714
09/24/2004
FIDJI-VERTEBRAL BODY REPLACEMENT TYPE 1, 2, 3 AND 4
SPINE NEXT AMERICA CORPORATION
K042713
09/30/2004
FIDJI-VERTEBRAL BODY REPLACEMENT TYPE 5
SPINE NEXT AMERICA CORPORATION
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