Medical Device Manufacturer · US , Bartlett , TN

Spinal Innovations, LLC - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2000
4
Total
4
Cleared
0
Denied

Spinal Innovations, LLC has 4 FDA 510(k) cleared medical devices. Based in Bartlett, US.

Historical record: 4 cleared submissions from 2000 to 2002. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Spinal Innovations, LLC
4 devices
1-4 of 4
Cleared Dec 06, 2002
SPECTRUM CERVICAL SPINAL SYSTEM
K022997 · KWQ
Orthopedic · 88d
Cleared Jan 30, 2002
ASCEND SPINAL FIXATION SYSTEM WITH THE SHADOW SPINAL SYSTEM
K013196 · KWP
Orthopedic · 127d
Cleared May 30, 2001
CONVERGENCE CERVICAL SPINAL SYSTEM
K010639 · KWQ
Orthopedic · 86d
Cleared Oct 05, 2000
ASCEND SPINAL FIXATION SYSTEM
K002069 · KWP
Orthopedic · 90d
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