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FDA 510(k) clearance · back to tracker

Stereotaxic Guiding Surgical Devices, NaoTrac S

Brain Navi Biotechnology Co., Ltd. cleared K242575 on 2025-05-23, decision: substantially equivalent

K-number

K242575

Sponsor

Brain Navi Biotechnology Co., Ltd.

Device

Stereotaxic Guiding Surgical Devices, NaoTrac S

Class

Class II

Decision

Substantially Equivalent

Decision date

2025-05-23

Product code

HAW

Advisory committee

Neurology

Medical specialty

Neurology

Regulation number

882.4560

Official FDA record

Open K242575on accessdata.fda.gov →

FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.

openFDA JSON

Raw record →

Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.

Use this as a predicate

Drop K242575 into Compass and start a substantial-equivalence draft.

Compass pulls the predicate's intended use, technological characteristics, and performance data, maps them against your device, and produces a draft SE table aligned to FDA's 510(k) program guidance.

Try the sandbox

Source

Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.