KT2000 KNEE LIGAMENT ARTHROMETER— 510(k) K942059

Name: FDA 510(k) clearance K942059
Creator: U.S. Food and Drug Administration
Published: 1994-09-20

Substantially Equivalent

Medmetric Corp.

FDA 510(k) clearance K942059 for KT2000 KNEE LIGAMENT ARTHROMETER, Substantially Equivalent on 1994-09-20. Applicant: Medmetric Corp.. Device class: 1.

Clearance details

Applicant: Medmetric Corp.
Product code: Code LYH
Device class: Class 1
Regulation: 21 CFR 890.1615
Advisory panel: Physical Medicine
Date received: 1994-04-29
Decision date: 1994-09-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.