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Spinecraft, LLC

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5
Categories4
Latest FDA decision2023-07-20
TypeNumberDevice NameCodeDateActions
510(k) K223301 ASTRA & AVANT Navigation Instruments System and ASTRA-OCT Navigation Instruments SystemOLO2023-07-20 View
510(k) K223273 ASTRA Spine SystemNKB2022-12-22 View
510(k) K211935 ORIO-Ti Intervertebral Body Fusion Cage SystemODP2021-09-30 View
510(k) K211323 ASTRA Spine SystemNKB2021-06-03 View
510(k) K181350 ASTRA-OCT Spine SystemNKG2018-07-06 View
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