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Wenzel Spine, Inc.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories4
Latest FDA decision2025-07-09
TypeNumberDevice NameCodeDateActions
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
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