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FDA 510(k) Applications for Medical Device Product Code "ORR"
FDA 510(k) Number
Applicant
Device Name
Decision Date
K171257
MRI Interventions, Inc.
ClearPoint System
10/20/2017
K181195
MRI Interventions, Inc.
ClearPoint System
11/02/2018
K111073
SURGI-VISION, INC.
SURGIVISION INC. CLEARPOINT SYSTEM
06/22/2011
K100836
SURGIVISION, INC.
CLEARPOINT SYSTEM
06/16/2010
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