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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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