Medical Device Manufacturer · US , Pleasant Hill , CA

Lanx, LLC - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 2004
13
Total
13
Cleared
0
Denied

Lanx, LLC has 13 FDA 510(k) cleared orthopedic devices. Based in Pleasant Hill, US.

Historical record: 13 cleared submissions from 2004 to 2012.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Lanx, LLC
13 devices
1-13 of 13
Cleared Mar 09, 2012
LANX SPINAL FIXATION SYSTEM
K120399 · NKB
Orthopedic · 30d
Cleared Feb 10, 2011
LANX FUSION SYSTEM
K102738 · OVD
Orthopedic · 141d
Cleared Feb 08, 2011
LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)
K103040 · NKB
Orthopedic · 118d
Cleared Dec 10, 2009
MODIFICATION TO LANX SPINAL FIXATION SYSTEM
K093285 · MNI
Orthopedic · 51d
Cleared Oct 21, 2008
LANX CERVICAL INTERVERTEBRAL BODY FUSION DEVICE
K082774 · MAX
Orthopedic · 29d
Cleared Jan 24, 2008
LANX INTERVERTEBRAL BODY FUSION DEVICE
K073144 · MAX
Orthopedic · 78d
Cleared Dec 28, 2007
POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)
K071905 · KWQ
Orthopedic · 171d
Cleared Sep 17, 2007
LANX SPINAL FIXATION SYSTEM
K071877 · MNI
Orthopedic · 70d
Cleared Aug 15, 2007
LANX DEFORMITY SYSTEM
K071633 · KWP
Orthopedic · 62d
Cleared Oct 07, 2005
LANX VBR SYSTEM
K052384 · MQP
Orthopedic · 38d
Cleared May 16, 2005
LANX SPINAL FIXATION SYSTEM
K043484 · MNI
Orthopedic · 150d
Cleared Apr 11, 2005
LANX ANTERIOR CERVICAL PLATE SYSTEM
K050774 · KWQ
Orthopedic · 17d
Cleared Apr 12, 2004
LANX ANTERIOR CERVIAL PLATE SYSTEM
K040401 · KWQ
Orthopedic · 55d
Filters
Filter by Specialty
All13 Orthopedic 13