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FDA 510(k) Application Details - K090375
Device Classification Name
Orthopedic Stereotaxic Instrument
More FDA Info for this Device
510(K) Number
K090375
Device Name
Orthopedic Stereotaxic Instrument
Applicant
AESCULAP IMPLANT SYSTEM, INC.
3773 Corporate Parkway
Center Valley, PA 18034 US
Other 510(k) Applications for this Company
Contact
LISA M BOYLE
Other 510(k) Applications for this Contact
Regulation Number
882.4560
More FDA Info for this Regulation Number
Classification Product Code
OLO
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
02/17/2009
Decision Date
06/23/2009
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
OR - Orthopedic
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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