FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

Stereotaxic Guiding Surgical Devices, NaoTrac S

K Number: K242575 · Decision May 23, 2025
Classifications
1
FEI Numbers
246
Registration Numbers
246
Same Product Code
417
Applicant Total
1
Review Days
267

Basic Information

Device Name
Stereotaxic Guiding Surgical Devices, NaoTrac S
K Number
K242575
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Brain Navi Biotechnology Co., Ltd.
Date Received
August 29, 2024
Decision Date
May 23, 2025
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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