FDA 510(k) Application Details - K950577

Device Classification Name Implant, Endosseous, Root-Form

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510(K) Number K950577
Device Name Implant, Endosseous, Root-Form
Applicant CORE-VENT CORP.
4630 SOUTH ARVILLE
STE D
LAS VEGAS, NV US
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Contact GLEN NEALLY
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Regulation Number 872.3640

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Classification Product Code DZE
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Date Received 01/27/1995
Decision Date 07/11/1995
Decision SE - Substantially Equivalent
Classification Advisory Committee DE - Dental
Review Advisory Committee DE - Dental
Statement / Summary / Purged Status Statement
Type Traditional
Reviewed By Third Party N
Expedited Review



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