Medical Device Manufacturer · US , Washington, Dc , DC

Nlt Spine, Ltd. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2011
8
Total
8
Cleared
0
Denied

Nlt Spine, Ltd. has 8 FDA 510(k) cleared medical devices. Based in Washington, Dc, US.

Historical record: 8 cleared submissions from 2011 to 2016. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Nlt Spine, Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Nlt Spine, Ltd.
8 devices
1-8 of 8
Cleared Sep 15, 2016
PROW FUSION-L
K153665 · MAX
Orthopedic · 269d
Cleared Jul 11, 2016
PROW FUSION-V
K153786 · MAX
Orthopedic · 193d
Cleared Jul 17, 2015
PROW FUSION
K151654 · MAX
Orthopedic · 29d
Cleared Nov 27, 2013
ESPIN SYSTEM
K133061 · HRX
Orthopedic · 61d
Cleared Oct 16, 2013
PROW FUSION
K130254 · MAX
Orthopedic · 257d
Cleared Feb 07, 2013
ESPIN
K130057 · HRX
Orthopedic · 29d
Cleared Aug 09, 2012
ESPIN
K120553 · HRX
Orthopedic · 168d
Cleared Nov 08, 2011
PROW FUSION
K112359 · MAX
Orthopedic · 84d
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