FDA 510(k) Applications Submitted by CAROL LAUSTER
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K010212 | 01/23/2001 | OFFSET TIBIAL TRAY | BIOMET, INC. |
| K001581 | 05/22/2000 | LACTOSORB 5.0 MM WASHER | BIOMET, INC. |
| K003131 | 10/06/2000 | MODIFICATION TO: RADIOLUCENT COLLES FRACTURE KIT | BIOMET, INC. |
| K003281 | 10/19/2000 | LACTOSORB RAPIDFLAP | BIOMET, INC. |
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