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FDA 510(k) Application Details - K093975
Device Classification Name
Abutment, Implant, Dental, Endosseous
More FDA Info for this Device
510(K) Number
K093975
Device Name
Abutment, Implant, Dental, Endosseous
Applicant
PAN GLOBAL IMPLANT
#404, 1023 WOLFE AVE
VANCOUVER, BC V6H 1V6 CA
Other 510(k) Applications for this Company
Contact
HAROLD BERGMAN
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
12/24/2009
Decision Date
06/04/2010
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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