FDA 510(k) Applications Submitted by MANDY COE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K090313 | 02/09/2009 | PIGALILEO TKR BASE V2.3 AND CAS V4.1 | SMITH & NEPHEW, INC. |
| K090982 | 04/07/2009 | SMITH & NEPHEW HIP SYSTEMS WITH HA | SMITH & NEPHEW, INC. |
| K083762 | 12/18/2008 | BIOLOX DELTA CERAMIC FEMORAL HEADS | SMITH & NEPHEW, INC. |
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