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FDA 510(k) Application Details - K210855
Device Classification Name
Implant, Endosseous, Root-Form
More FDA Info for this Device
510(K) Number
K210855
Device Name
Implant, Endosseous, Root-Form
Applicant
Institut Straumann AG
Peter Merian Weg 12
Basel CH-4002 CH
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Contact
Viviana Horhoiu
Other 510(k) Applications for this Contact
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
03/23/2021
Decision Date
06/21/2021
Decision
SESE - SUBST EQUIV
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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