FDA 510(k) Applications Submitted by TINA LAKIN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K000262 | 01/28/2000 | BOHN FEMORAL COMPONENT | BIOMET MANUFACTURING, INC. |
| K001010 | 03/29/2000 | ASCENT KNEE REVISION FEMORAL STEM | BIOMET, INC. |
| K001580 | 05/22/2000 | GROSS FEMORAL COMPONENT | BIOMET, INC. |
| K002757 | 09/05/2000 | ONCOLOGY SALVAGE SYSTEM | BIOMET, INC. |
| K994007 | 11/24/1999 | MALLORY/HEAD SMOOTH FEMORAL COMPONENT | BIOMET, INC. |
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