FDA 510(k) Applications Submitted by ANDREW LAMBORNE
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K100191 |
01/22/2010 |
LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS) |
LANX, INC. |
| K090252 |
02/02/2009 |
MODIFICATION TO: LANX SPINAL FIXATION SYSTEM |
LANX, INC. |
| K090300 |
02/06/2009 |
MODIFICATION TO AUTOFUSER |
ACE MEDICAL US, LLC |
| K090316 |
02/09/2009 |
MODIFICATION TO: LANX ANTERIOR CERVICAL PLATE SYSTEM |
LANX, INC. |
| K100935 |
04/05/2010 |
LANX SPINAL FIXATION SYSTEM |
LANX, INC. |
| K092656 |
08/28/2009 |
LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM |
LANX, INC. |
| K103091 |
10/19/2010 |
LANX SPINAL FIXATION SYSTEM |
LANX, INC. |
| K093285 |
10/20/2009 |
MODIFICATION TO LANX SPINAL FIXATION SYSTEM |
LANX, LLC |
| K083581 |
12/04/2008 |
LANX SPINAL FIXATION SYSTEM |
LANX, INC. |
| K033039 |
09/29/2003 |
MODIFICATION TO: ACCUFUSER, ACCUFUSER PLUS, STANDARD PROCEDURE KITS |
MCKINLEY, INC. |
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