KADANCE 2000— 510(k) K012492

Substantially Equivalent

Kada Research, Inc.

FDA 510(k) clearance K012492 for KADANCE 2000, Substantially Equivalent on 2001-11-02. Applicant: Kada Research, Inc.. Device class: 2.

Clearance details

Applicant: Kada Research, Inc.
Product code: Code LBB
Device class: Class 2
Regulation: 21 CFR 888.1240
Advisory panel: Orthopedic
Date received: 2001-08-03
Decision date: 2001-11-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, 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.