FDA 510(k) Applications Submitted by RICHARD W WOODS
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K080302 |
02/05/2008 |
CAYMAN BUTTRESS PLATE SYSTEM |
K2M, INC. |
K092211 |
07/22/2009 |
CHESAPEAKE SPINAL SYSTEM |
K2M, INC. |
K082698 |
09/15/2008 |
ALEUTIAN IBF SYSTEM |
K2M, INC. |
K080024 |
01/04/2008 |
ALEUTIAN SPACER, MODEL K2-07-1004-01, K2-07-1005-01 |
K2M, INC. |
K100061 |
01/11/2010 |
CAYMAN SCREWS MODEL K2-12-1000-XX, K2-12-1001-XX |
K2M, INC. |
K070229 |
01/24/2007 |
RANGE SPINAL SYSTEM |
K2M, INC. |
K080611 |
03/04/2008 |
MESA SPINAL SYSTEM |
K2M, INC. |
K080792 |
03/20/2008 |
K2M COCR ROD |
K2M, INC. |
K081107 |
04/18/2008 |
CASPIAN SPINAL SYSTEM, SCREWS, RODS, HOOKS, ROD CONNECTORS |
K2M, INC. |
K091253 |
04/29/2009 |
THORACOLUMBAR PLATE, MODEL 1208-41FXX, LUMBER PLATE, MODEL 1208-41FXXL, SACRAL PLATE, MODEL 1208-41FXXS |
K2M, INC. |
K081380 |
05/16/2008 |
THORACOLUMBAR, LUMBAR AND SACRAL PLATES AND 6.0 AND 7.0 MM BONE SCREWS |
K2M, INC. |
K081381 |
05/16/2008 |
RANGE SPINAL SYSTEM, LARGE DENALI SCREWS |
K2M, INC. |
K092474 |
08/12/2009 |
PYRENEES CERVICAL PLATE SYSTEM, SEMI-CONSTRAINED SCREWS |
K2M, INC. |
K092640 |
08/27/2009 |
CASPIAN SPINAL SYSTEM |
K2M, INC. |
K052398 |
08/31/2005 |
MESA SPINAL SYSTEM |
K2M, LLC |
K052404 |
09/01/2005 |
DENALI DEFORMITY SYSTEM |
K2M, LLC |
K082769 |
09/22/2008 |
MESA AND RANGE SPINAL SYSTEMS |
K2M, INC. |
K042635 |
09/27/2004 |
DENALI SPINE SYSTEM |
K2M, LLC |
K072914 |
10/12/2007 |
NATURAL BRIDGE LP TRANSVERSE CONNECTORS |
K2M, INC. |
K014164 |
12/19/2001 |
GREAT TOE IMPLANT SYSTEM |
HARMOS ORTHOPAEDICS, INC. |
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