FDA 510(k) Application Details - K970817

Device Classification Name Staple, Implantable

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510(K) Number K970817
Device Name Staple, Implantable
Applicant BIOPSYS MEDICAL, INC.
3 MORGAN
IRVINE, CA 92618 US
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Contact MARK A COLE
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Regulation Number 878.4750

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Classification Product Code GDW
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Date Received 03/06/1997
Decision Date 09/11/1997
Decision SESE - SUBST EQUIV
Classification Advisory Committee SU - General & Plastic Surgery
Review Advisory Committee SU - General & Plastic Surgery
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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