ACCIN PATELLOFEMORAL SYSTEM— 510(k) K073120

Name: FDA 510(k) clearance K073120
Creator: U.S. Food and Drug Administration
Published: 2008-02-29

Substantially Equivalent

Accelerated Innovation, LLC

FDA 510(k) clearance K073120 for ACCIN PATELLOFEMORAL SYSTEM, Substantially Equivalent on 2008-02-29. Applicant: Accelerated Innovation, LLC. Device class: 2.

Clearance details

Applicant: Accelerated Innovation, LLC
Product code: Code KRR
Device class: Class 2
Regulation: 21 CFR 888.3540
Advisory panel: Orthopedic
Date received: 2007-11-05
Decision date: 2008-02-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clifton, NJ, 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.