PARALLAX EZFLOW CEMENT DELIVERY SYSTEM— 510(k) K051820

Name: FDA 510(k) clearance K051820
Creator: U.S. Food and Drug Administration
Published: 2005-09-06

Substantially Equivalent

Arthrocare Corp.

FDA 510(k) clearance K051820 for PARALLAX EZFLOW CEMENT DELIVERY SYSTEM, Substantially Equivalent on 2005-09-06. Applicant: Arthrocare Corp.. Device class: 1.

Clearance details

Applicant: Arthrocare Corp.
Product code: Code OAR
Device class: Class 1
Regulation: 21 CFR 888.4200
Advisory panel: Orthopedic
Date received: 2005-07-05
Decision date: 2005-09-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sunnyvale, CA, US

Download summary PDF View on FDA.gov ↗

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