FDA 510(k) Application Details - K001466

Device Classification Name System, Vocal Cord Medialization

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510(K) Number K001466
Device Name System, Vocal Cord Medialization
Applicant SMITH & NEPHEW, INC.
2925 APPLING RD.
BARTLETT, TN 38133 US
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Contact ALICIA E FARAGE
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Regulation Number 874.3620

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Classification Product Code MIX
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Date Received 05/10/2000
Decision Date 07/26/2000
Decision SESE - SUBST EQUIV
Classification Advisory Committee EN - Ear, Nose, & Throat
Review Advisory Committee EN - Ear, Nose, & Throat
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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