FDA 510(k) Applications Submitted by MICHAELA NORRIS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K121835 | 06/22/2012 | DOMED TRI-PEG PATELLA, HIGHLY CROSS LINKED DOMED TRI-PEG PATELLA WITH VE | ENCORE MEDICAL, L.P. |
| K123982 | 12/26/2012 | TURON GLENOID PEGGED, E+, TURON KEELED GLENOID, E+ | ENCORE MEDICAL, L.P. |
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