FDA 510(k) clearance · back to tracker

ARVIS Surgical Navigation System

Kico Knee Innovation Company Pty Limited cleared K243980 on 2025-03-21, decision: substantially equivalent

K-number

K243980

Sponsor

Kico Knee Innovation Company Pty Limited

Device

ARVIS Surgical Navigation System

Class

Class II

Decision

Substantially Equivalent

Decision date

2025-03-21

Product code

SBF

Advisory committee

Neurology

Medical specialty

Neurology

Regulation number

882.4560

Official FDA record

Open K243980on accessdata.fda.gov →

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

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Raw record →

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

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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.

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Source

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