PTA (PROGRESSIVE TIBIAL ALIGNMENT)— 510(k) K060403

Name: FDA 510(k) clearance K060403
Creator: U.S. Food and Drug Administration
Published: 2006-03-28

Substantially Equivalent

Meridian Medical

FDA 510(k) clearance K060403 for PTA (PROGRESSIVE TIBIAL ALIGNMENT), Substantially Equivalent on 2006-03-28. Applicant: Meridian Medical. Device class: 2.

Clearance details

Applicant: Meridian Medical
Product code: Code LXT
Device class: Class 2
Regulation: 21 CFR 888.3030
Advisory panel: Orthopedic
Date received: 2006-02-15
Decision date: 2006-03-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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