FDA 510(k) clearance · back to tracker

TruVision Single-Use 1.9mm Arthroscopy System

Nexus CMF, LLC cleared K260156 on 2026-10-09, decision: substantially equivalent

K-number

K260156

Sponsor

Nexus CMF, LLC

Device

TruVision Single-Use 1.9mm Arthroscopy System

Class

Class II

Decision

Substantially Equivalent

Decision date

2026-10-09

Product code

HRX

Advisory committee

Orthopedic

Medical specialty

Orthopedic

Regulation number

888.1100

Official FDA record

Open K260156on 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.

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Drop K260156 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.

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Source

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