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FDA 510(k) Application Details - K050478
Device Classification Name
Implant, Endosseous, Root-Form
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510(K) Number
K050478
Device Name
Implant, Endosseous, Root-Form
Applicant
MEDICON, E.G.
GAENSAECKER 15
TUTTLINGEN D-78532 DE
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Contact
JOACHIM SCHMID
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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
02/24/2005
Decision Date
06/15/2005
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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