FDA 510(k) Applications Submitted by BRUCE WALDON
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K010839 | 03/21/2001 | CLS VARUS STEM/CLS 135 STEM | SULZER ORTHOPEDICS, INC. |
| K011954 | 06/22/2001 | SULZER ORTHOPEDICS ALLEGRETTO UNICOMPARTMENTAL KNEE | SULZER ORTHOPEDICS, INC. |
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