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FDA 510(k) Application Details - K002871
Device Classification Name
Clip, Aneurysm
More FDA Info for this Device
510(K) Number
K002871
Device Name
Clip, Aneurysm
Applicant
AESCULAP, INC.
3773 EXECUTIVE CENTER PKWY.
CENTER VALLEY, PA 18034 US
Other 510(k) Applications for this Company
Contact
JOYCE THOMAS
Other 510(k) Applications for this Contact
Regulation Number
882.5200
More FDA Info for this Regulation Number
Classification Product Code
HCH
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/14/2000
Decision Date
10/13/2000
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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