Wenzel Spine
Wenzel Spine appears in FDA public data with 0 recalls, 10 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 26, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 10
- Inspections
- 3
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K262595 | VariLift-C Cervical Interbody Fusion System | August 26, 2026 |
| K250247 | panaSIa SI Fusion System | July 9, 2025 |
| K231076 | VariLift®-C Interbody Fusion System | September 27, 2023 |
| K231807 | primaLOK SP Interspinous Fusion System | August 15, 2023 |
| K180822 | VariLift-LX Interbody Fusion System, VariLift-C Interbody Fusion System | January 28, 2019 |
| K151900 | VariLift-L Interbody Fusion Device | December 11, 2015 |
| K131296 | VARILIFT-L INTERBODY FUSION DEVICE | September 3, 2013 |
| K120603 | VARILIFT -C | January 29, 2013 |
| K111123 | VARILIFT CERVICAL INTERBODY FUSION SYSTEM | December 8, 2011 |
| K100820 | WENZEL SPINE VARILIFT INTERBODY FUSION SYSTEM | August 5, 2010 |