FDA 510(k) Applications Submitted by LANX, LLC
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K082774 |
09/22/2008 |
LANX CERVICAL INTERVERTEBRAL BODY FUSION DEVICE |
LANX, LLC |
| K102738 |
09/22/2010 |
LANX FUSION SYSTEM |
LANX, LLC |
| K093285 |
10/20/2009 |
MODIFICATION TO LANX SPINAL FIXATION SYSTEM |
LANX, LLC |
| K103040 |
10/13/2010 |
LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS) |
LANX, LLC |
| K040401 |
02/17/2004 |
LANX ANTERIOR CERVIAL PLATE SYSTEM |
LANX, LLC |
| K050774 |
03/25/2005 |
LANX ANTERIOR CERVICAL PLATE SYSTEM |
LANX, LLC |
| K052384 |
08/30/2005 |
LANX VBR SYSTEM |
LANX, LLC |
| K043484 |
12/17/2004 |
LANX SPINAL FIXATION SYSTEM |
LANX, LLC |
| K073144 |
11/07/2007 |
LANX INTERVERTEBRAL BODY FUSION DEVICE |
LANX, LLC |
| K071633 |
06/14/2007 |
LANX DEFORMITY SYSTEM |
LANX, LLC |
| K071877 |
07/09/2007 |
LANX SPINAL FIXATION SYSTEM |
LANX, LLC |
| K071905 |
07/10/2007 |
POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS) |
LANX, LLC |
| K120399 |
02/08/2012 |
LANX SPINAL FIXATION SYSTEM |
LANX, LLC |
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