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.

Life Spine, Inc.

FDA 510(k) & PMA Approved Devices — 66 products

Total Devices66
Categories14
Latest FDA decision2026-07-28
TypeNumberDevice NameCodeDateActions
510(k) K212903 SIMPACT Sacroiliac Joint Fixation SystemOUR2021-12-15 View
510(k) K212520 ProLift Micro Expandable Spacer SystemMAX2021-10-08 View
510(k) K202836 GX Navigation Instrument SystemOLO2021-08-19 View
510(k) K210061 ProLift Lateral HELO FixatedMAX2021-04-30 View
510(k) K210549 ARx Spinal SystemNKB2021-04-22 View
510(k) K203361 ProLift Wedge Expandable Spacer SystemMAX2021-03-17 View
510(k) K203163 ARx Illiac Spinal Screw SystemNKB2020-12-17 View
510(k) K201538 Life Spine SIMPACT Sacroiliac Joint Fixation SystemOUR2020-09-18 View
510(k) K201721 TruLift Expandable Spacer SystemMAX2020-09-04 View
510(k) K201500 Life Spine Plateau-A Ti Anterior Lumbar Spacer & Plateau-X Ti Lateral Lumbar SpacerMAX2020-08-04 View
510(k) K200896 Solstice CCINKG2020-04-28 View
510(k) K200070 ARx Spinal SystemNKB2020-04-23 View
510(k) K200338 ProLift Lateral FixatedOVD2020-04-17 View
510(k) K193521 Steerable Plateau TiMAX2020-02-06 View
510(k) K193258 ProLift Expandable SystemMAX2020-01-31 View
510(k) K191834 Stand-Alone ALIF Titanium SystemOVD2019-12-16 View
510(k) K190721 LongBow TiMAX2019-11-14 View
510(k) K191927 Hinged Laminoplasty SystemNQW2019-09-20 View
510(k) K191575 ARx Spinal SystemNKB2019-08-08 View
510(k) K190488 ProLift Expandable SystemMAX2019-07-23 View

Page 2 of 4

↑