Medical Device Manufacturer · US , Round Rock , TX

Verticor, Ltd. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2009

Recent clearances: VERTICOR K-WIRE SYSTEM, VENUS ANTERIOR CERVICAL PLATE, CERVICORE CORPECTOMY CAGE

View 3 510(k) Devices ↓

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Verticor, Ltd. Orthopedic ✕

3 devices

1-3 of 3

Cleared Feb 28, 2011

VERTICOR K-WIRE SYSTEM

Orthopedic · 53d

Cleared Feb 10, 2011

VENUS ANTERIOR CERVICAL PLATE

Orthopedic · 108d

Cleared Dec 23, 2009

CERVICORE CORPECTOMY CAGE

Orthopedic · 224d