FDA 510(k) Applications Submitted by HOWMEDICA OSTEONICS CORP. DBA STRYKER ORTHOPEADICS

FDA 510(k) Number Submission Date Device Name Applicant
K111065 04/18/2011 STRYKER (R) PATIENT SPECIFIC POLYMER IMPLANT HOWMEDICA OSTEONICS CORP. DBA STRYKER ORTHOPEADICS


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