Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Spinecraft, LLC

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10
Categories0
Latest FDA decision
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
510(k) K131521 VELOX ANTERIOR CERVICAL PLATE SYSTEMKWQ2013-12-24 View
510(k) K132603 APEX SPINE SYSTEMNKB2013-11-20 View
510(k) K110906 APEX SPINE SYSTEMNKB2011-07-26 View
510(k) K103505 ALTUM ANTERIOR CERVICAL PLATEKWQ2011-03-15 View
510(k) K102488 APEX SPINE SYSTEM W/ COCR RODSMNH2010-12-10 View
↑