FDA 510(k) Applications Submitted by Tim Crabtree
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K140116 |
01/16/2014 |
RESTORELLE Y CONTOUR MESH |
COLOPLAST A/S |
| K030193 |
01/21/2003 |
ADVANCE LESS CONFORMING TIBIAL COMPONENT |
WRIGHT MEDICAL TECHNOLOGY, INC. |
| K060638 |
03/10/2006 |
DYNESYS SPINAL SYSTEM WITH HA COATED SCREWS |
ZIMMER SPINE, INC |
| K151020 |
04/16/2015 |
Rampart-T Interbody Fusion System |
Spineology, Inc. |
| K011299 |
04/30/2001 |
SMITH AND NEPHEW 5.00MM ABSORBABLE POLYMER ANCHOR |
SMITH & NEPHEW, INC. |
| K111233 |
05/02/2011 |
SUPRIS RETROPUBIC SLING SYSTEM |
COLOPLAST A/S |
| K061353 |
05/15/2006 |
TRINICA ANTERIOR LUMBAR PLATE SYSTEM |
ZIMMER SPINE, INC. |
| K101704 |
06/17/2010 |
ZIMMER DTO PIN PRESS INSTRUMENT |
ZIMMER SPINE, INC. |
| K121833 |
06/22/2012 |
OSTOMY IRRIGATION SET |
COLOPLAST A/S |
| K011985 |
06/26/2001 |
SMITH & NEPHEW PHOENIX 5.0 ALLOGRAFT ANCHOR KIT |
SMITH & NEPHEW, INC. |
| K132061 |
07/03/2013 |
RESTORELLE M, RESTORELLE XL |
COLOPLAST CORP. |
| K012314 |
07/23/2001 |
DYONICS ELECTROBLADE RESECTOR |
SMITH & NEPHEW, INC. |
| K072183 |
08/06/2007 |
ST360 SPINAL FIXATION SYSTEM, MODEL 07.0029-7500.5600 |
ZIMMER SPINE, INC. |
| K122440 |
08/10/2012 |
RESTORELLE L |
COLOPLAST CORP. |
| K112322 |
08/12/2011 |
RESTORELLE POLYPROPYLENE Y MESH |
COLOPLAST A/S |
| K142213 |
08/12/2014 |
VIA SPINOUS PROCESS FIXATION SYSTEM |
SPINEOLOGY, INC. |
| K112386 |
08/18/2011 |
EXAIR ANTERIOR AND POSTERIOR PROLAPSE REPAIR SYSTEM |
COLOPLAST CORP. |
| K042702 |
09/30/2004 |
SILHOUETTE SPINAL FIXATION SYSTEM |
ZIMMER SPINE, INC. |
| K143403 |
11/28/2014 |
Threshold Pedicular Fixation System |
Spineology, Inc. |
| K123914 |
12/19/2012 |
RESTORELLE Y CONTOUR |
COLOPLAST A/S |
| K043565 |
12/27/2004 |
MODIFICATION TO DYNESYS SPINAL SYSTEM |
ZIMMER SPINE, INC |
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