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K&J Consulting Corp.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories3
Latest FDA decision2023-11-27
TypeNumberDevice NameCodeDateActions
510(k) K233332 Statera-C™ Spinal SystemNKG2023-11-27 View
510(k) K232586 Rexious Spinal Fixation System, Statera™ Spinal System, Statera-M™ Spinal SystemNKB2023-10-24 View
510(k) K231460 FORTIS and HANA Anterior Cervical Plate System, Rex Anterior Cervical Plate System, BALTEUM™ & BALTEUM-ONE™ Lumbar Plate System, and Osprey™ Anterior Cervical Plate SystemKWQ2023-07-16 View
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