Medical Device Manufacturer · US , Austin , TX

Wenzel Spine - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2010

Recent clearances: VARILIFT -C, VARILIFT CERVICAL INTERBODY FUSION SYSTEM, WENZEL SPINE VARILIFT INTERBODY FUSION SYSTEM

View 3 510(k) Devices ↓
3
Total
3
Cleared
0
Denied

FDA 510(k) Regulatory Record - Wenzel Spine Orthopedic ✕

3 devices
1-3 of 3
Cleared Jan 29, 2013
VARILIFT -C
K120603 · ODP
Orthopedic · 336d
Cleared Dec 08, 2011
VARILIFT CERVICAL INTERBODY FUSION SYSTEM
K111123 · ODP
Orthopedic · 231d
Cleared Aug 05, 2010
WENZEL SPINE VARILIFT INTERBODY FUSION SYSTEM
K100820 · MAX
Orthopedic · 135d
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