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Spine Next America Corporation

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K042714 FIDJI-VERTEBRAL BODY REPLACEMENT TYPE 1, 2, 3 AND 4MQP2004-12-29 View
510(k) K042713 FIDJI-VERTEBRAL BODY REPLACEMENT TYPE 5MQP2004-12-29 View
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