Medical Device Manufacturer · US , Chicago , IL

Meditech Advisors, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2009
2
Total
2
Cleared
0
Denied

Meditech Advisors, LLC has 2 FDA 510(k) cleared medical devices. Based in Chicago, US.

Historical record: 2 cleared submissions from 2009 to 2013. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Meditech Advisors, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Meditech Advisors, LLC
2 devices
1-2 of 2
Cleared Mar 28, 2013
TALOS-C CERVICAL INTERVERTEBRAL BODY FUSION DEVICES
K122850 · ODP
Orthopedic · 191d
Cleared Jul 15, 2009
TALOS INTERVERTEBRAL BODY FUSION DEVICE
K090707 · MAX
Orthopedic · 120d
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