FDA 510(k) Application Details - K770146

Device Classification Name Crutch

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510(K) Number K770146
Device Name Crutch
Applicant MADDAK, INC.

, US
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Regulation Number 890.3150

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Classification Product Code IPR
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Date Received 01/24/1977
Decision Date 01/28/1977
Decision SE - Substantially Equivalent
Classification Advisory Committee PM - Physical Medicine
Review Advisory Committee PM - Physical Medicine
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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