FDA 510(k) Application Details - K864734

Device Classification Name Implant, Endosseous, Root-Form

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510(K) Number K864734
Device Name Implant, Endosseous, Root-Form
Applicant HALL SURGICAL, DIVISION OF ZIMMER, INC.
P.O. BOX 899
`ANTA BARBARA, CA US
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Contact DAVID D WELLINGTON
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Regulation Number 872.3640

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Classification Product Code DZE
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Date Received 12/04/1986
Decision Date 02/10/1987
Decision SE - Substantially Equivalent
Classification Advisory Committee EN - Ear, Nose, & Throat
Review Advisory Committee DE - Dental
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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