FDA 510(k) Applications Submitted by SHEREEN MYERS
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K110069 |
01/10/2011 |
SMITH & NEPHEW, INC SPATIALFRAME V4.1 WEB-BASED SOFTWARE |
SMITH & NEPHEW, INC. |
| K110101 |
01/13/2011 |
TAPER OXINIUM FEMORAL HEAD |
SMITH & NEPHEW, INC. |
| K110240 |
01/27/2011 |
SMITH & NEPHEW, INC. SURESHOT DISTAL TARGETING SYSTEM V2.1 |
SMITH & NEPHEW, INC. |
| K090656 |
03/12/2009 |
INTERTAN CHS LIMITED COLLAPSE SET SCREW |
SMITH & NEPHEW, INC. |
| K100795 |
03/22/2010 |
JET-X BAR SYSTEM CLAMPS AND POSTS REPROCESSING |
SMITH & NEPHEW, INC. |
| K121443 |
05/15/2012 |
JOURNEY II CR KNEE SYSTEM |
SMITH & NEPHEW, INC. |
| K101499 |
06/01/2010 |
JOURNEY CR KNEE SYSTEM |
SMITH & NEPHEW, INC. |
| K111711 |
06/20/2011 |
JOURNEY II BCS KNEE SYSTEM |
SMITH & NEPHEW, INC. |
| K093047 |
09/30/2009 |
SMITH & NEPHEW CIRCULAR FIXATION SYSTEM |
SMITH & NEPHEW, INC. |
| K102967 |
10/05/2010 |
SMITH & NEPHEW, INC. SURESHOT DISTAL TARGETING SYSTEM V2.0.2 |
SMITH & NEWPHEW, INC |
| K113482 |
11/23/2011 |
JOURNEY II DEEP DISHED ARTICULAR INSERTS |
SMITH & NEPHEW, INC. |
| K093991 |
12/24/2009 |
SLR-PLUS STANDARD AND LATERAL FEMORAL STEMS |
SMITH & NEPHEW, INC. |
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