FDA 510(k) Application Details - K770118

Device Classification Name Clamp

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510(K) Number K770118
Device Name Clamp
Applicant STRYKER CORP.

, US
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Regulation Number 878.4800

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Classification Product Code HXD
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Date Received 01/21/1977
Decision Date 01/26/1977
Decision SE - Substantially Equivalent
Classification Advisory Committee OR - Orthopedic
Review Advisory Committee SU - General & Plastic Surgery
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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