Medical Device Manufacturer · US , Washington, Dc , DC

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

8 submissions · 8 cleared · Since 2011

Recent clearances: PROW FUSION-L, PROW FUSION-V, PROW FUSION

View 8 510(k) Devices ↓
8
Total
8
Cleared
0
Denied

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

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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