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FDA 510(k) Application Details - K040205
Device Classification Name
Abutment, Implant, Dental, Endosseous
More FDA Info for this Device
510(K) Number
K040205
Device Name
Abutment, Implant, Dental, Endosseous
Applicant
INTRA-LOCK INTERNATIONAL
1200 NORTH FEDERAL HWY
SUITE 200
BOCA RATON, FL 33432 US
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Contact
JEFFERY SAKOFF
Other 510(k) Applications for this Contact
Regulation Number
872.3630
More FDA Info for this Regulation Number
Classification Product Code
NHA
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
01/30/2004
Decision Date
03/22/2004
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Abbreviated
Reviewed By Third Party
N
Expedited Review
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