Wenzel Spine, Inc.
Wenzel Spine, Inc. holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2026.
Top product codes for Wenzel Spine, Inc.
Recent clearances by Wenzel Spine, Inc.
- K262595 — VariLift-C Cervical Interbody Fusion System
- K250247 — panaSIa SI Fusion System
- K231076 — VariLift®-C Interbody Fusion System
- K231807 — primaLOK SP Interspinous Fusion System
- K180822 — VariLift-LX Interbody Fusion System, VariLift-C Interbody Fusion System
- K151900 — VariLift-L Interbody Fusion Device
- K131296 — VARILIFT-L INTERBODY FUSION DEVICE
Data sourced from openFDA. This site is unofficial and independent of the FDA.