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FDA 510(k) Application Details - K952996
Device Classification Name
Implant, Endosseous, Root-Form
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510(K) Number
K952996
Device Name
Implant, Endosseous, Root-Form
Applicant
IMPLANT CENTER OF THE PALM BEACHES
824 US HWY I, STE. 370
N. PALM BEACH, FL US
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Contact
JACK T KRAUSER
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Regulation Number
872.3640
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Classification Product Code
DZE
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More FDA Info for this Product Code
Date Received
06/23/1995
Decision Date
10/31/1995
Decision
SE - Substantially Equivalent
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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