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FDA 510(k) Application Details - K130682
Device Classification Name
Screw, Fixation, Intraosseous
More FDA Info for this Device
510(K) Number
K130682
Device Name
Screw, Fixation, Intraosseous
Applicant
HAGER & MEISINGER GMBH
HANSEMANNSTRASSE 10
NEUSS D-41468 DE
Other 510(k) Applications for this Company
Contact
WIEBKE STOLTEN
Other 510(k) Applications for this Contact
Regulation Number
872.4880
More FDA Info for this Regulation Number
Classification Product Code
DZL
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
03/13/2013
Decision Date
08/13/2013
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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