FDA 510(k) Applications Submitted by JANET JOHNSON AKIL
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K040656 |
03/12/2004 |
MODIFICATION TO SMITH & NEPHEW INTRAMEDULLARY HIP SCREW |
SMITH & NEPHEW, INC. |
| K052792 |
10/03/2005 |
ANTHOLOGY HIP STEM |
SMITH & NEPHEW, INC. |
| K042127 |
08/06/2004 |
SMITH & NEPHEW MODULAR HIP |
SMITH & NEPHEW, INC. |
| K032722 |
09/03/2003 |
TRIGEN STRAIGHT HUMERAL NAIL SYSTEM |
SMITH & NEPHEW, INC. |
| K042515 |
09/16/2004 |
SMITH & NEPHEW, INC. HIGH PERFORMANCE KNEE |
SMITH & NEPHEW, INC. |
| K033341 |
10/17/2003 |
SMITH & NEPHEW IMAGE GUIDED SURGICAL INSTRUMENTS FOR HIP APPLICATIONS |
SMITH & NEPHEW, INC. |
| K043052 |
11/05/2004 |
TRIGEN HINDFOOT FUSION NAIL |
SMITH & NEPHEW, INC. |
| K032683 |
08/29/2003 |
GENESIS II POROUS PLUS HA KNEE SYSTEM |
SMITH & NEPHEW, INC. |
| K023743 |
11/07/2002 |
SMITH & NEPHEW GLOBAL BIPOLAR SYSTEM |
SMITH & NEPHEW, INC. |
|
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