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.

Wenzel Spine, Inc.

FDA 510(k) & PMA Approved Devices — 6 products

Total Devices6
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K262595 VariLift-C Cervical Interbody Fusion SystemODP2026-08-26 View
510(k) K250247 panaSIa SI Fusion SystemOUR2025-07-09 View
510(k) K231076 VariLift®-C Interbody Fusion SystemODP2023-09-27 View
510(k) K231807 primaLOK™ SP Interspinous Fusion SystemPEK2023-08-15 View
510(k) K180822 VariLift-LX Interbody Fusion System, VariLift-C Interbody Fusion SystemMAX2019-01-28 View
510(k) K131296 VARILIFT-L INTERBODY FUSION DEVICEMAX2013-09-03 View
↑