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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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