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FDA 510(k) Application Details - K172219
Device Classification Name
Orthopedic Stereotaxic Instrument
More FDA Info for this Device
510(K) Number
K172219
Device Name
Orthopedic Stereotaxic Instrument
Applicant
MAKO Surgical Corp.
2555 Davie Road
Fort Lauderdale, FL 33317 US
Other 510(k) Applications for this Company
Contact
Karen Ariemma
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
07/24/2017
Decision Date
09/21/2017
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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