Medical Device Manufacturer · US , Broomfield , CO

Lanx, Inc. - FDA 510(k) Cleared Devices

23 submissions · 23 cleared · Since 2009
23
Total
23
Cleared
0
Denied
FDA 510(k) Regulatory Record - Lanx, Inc. Orthopedic ✕
23 devices
1-12 of 23
Cleared Jul 12, 2013
LANX FUSION SYSTEM
K131547 · OVD
Orthopedic · 44d
Cleared May 24, 2013
LANX SPINAL FIXATION SYSTEM
K131156 · KWP
Orthopedic · 30d
Cleared Mar 18, 2013
LANX FUSION SYSTEM- SA
K123767 · OVD
Orthopedic · 101d
Cleared Sep 10, 2012
LANX SPINAL FIZATION SYSTEM
K121316 · NKB
Orthopedic · 131d
Cleared Aug 17, 2012
LANX SPINAL FIXATION SYSTEM
K122145 · NKB
Orthopedic · 29d
Cleared Aug 02, 2012
LANX SPINAL FIXATION SYSTEM
K121940 · NKB
Orthopedic · 31d
Cleared Dec 19, 2011
LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)
K113434 · NKB
Orthopedic · 28d
Cleared Dec 16, 2011
LANX CERVICAL SA
K112388 · OVE
Orthopedic · 120d
Cleared Apr 15, 2011
LANX SPINAL FIXATION SYSTEM
K103091 · KWP
Orthopedic · 178d
Cleared Mar 25, 2011
LANX SPINAL SYSTEM
K103237 · NKB
Orthopedic · 143d
Cleared Mar 23, 2011
LANX LATERAL
K103666 · MAX
Orthopedic · 98d
Cleared Feb 28, 2011
LANX CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM
K103660 · ODP
Orthopedic · 75d
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