FDA 510(k) Applications Submitted by WESLEY JOHNSON
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K963700 | 09/16/1996 | METAGEN HIGH TIBIAL OSTEOTOMY SYSTEM | METAGEN, L.L.C. |
| K964003 | 10/07/1996 | METAGEN ALL POLY ACETABULAR CUP SYSTEM | METAGEN, L.L.C. |
| K983976 | 11/09/1998 | METAGEN ACTIVELOCK WIRE CERCLAGE SYSTEM | METAGEN, L.L.C. |
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