FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ClearPoint System

K Number: K160434 · Decision Mar 17, 2016
Classifications
1
FEI Numbers
250
Registration Numbers
250
Same Product Code
422
Applicant Total
14
Review Days
30

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Basic Information

Device Name
ClearPoint System
K Number
K160434
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mri Interventions, Inc.
Date Received
February 16, 2016
Decision Date
March 17, 2016
Product Code
HAW
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HAW Neurological Stereotaxic Instrument

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Other Clearances by Mri Interventions, Inc.

K Number Device Name
K200079 ClearPoint System and Accessories
K191701 Arcus Head Fixation Frame
K191400 Voyager Trajectory Array Guide (V-TAG)
K181731 MR Compatible Aspiration Kit
K181195 ClearPoint System
K171257 ClearPoint System
K160129 MRII Cranial Drill and Accessories
K142505 ClearPoint System
K151536 SmartTwist MRII Hand Drill, SmartTip MRII Drill bit Kit, 4.5mm, 6.0mm
K132436 VARIOGUIDE DRILL KIT
Search all 14 clearances from Mri Interventions, Inc. →