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

Neural Navigator

K Number: K191422 · Decision Apr 6, 2020
Classifications
1
FEI Numbers
250
Registration Numbers
250
Same Product Code
422
Applicant Total
6
Review Days
313

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Basic Information

Device Name
Neural Navigator
K Number
K191422
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Soterix Medical, Inc.
Date Received
May 29, 2019
Decision Date
April 6, 2020
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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K Number Device Name
K251653 SPRY TMS Therapy System (0550)
K233751 Milieve (YPS-301BD)
K234080 MEGA-IOM system with Neuro-IOM.NET software (32/B - 32/S - 16/S)
K192823 MEGA-TMS
K170291 IontoDC