FDA 510(k) Application Details - K033968

Device Classification Name Pin, Fixation, Smooth

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510(K) Number K033968
Device Name Pin, Fixation, Smooth
Applicant HOWMEDICA OSTEONICS CORP.
325 Corporate Drive
Mahwah, NJ 07430 US
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Contact VIVIAN KELLY
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Regulation Number 888.3040

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Classification Product Code HTY
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Date Received 12/22/2003
Decision Date 02/20/2004
Decision SESE - SUBST EQUIV
Classification Advisory Committee OR - Orthopedic
Review Advisory Committee OR - Orthopedic
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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