INTERPORE CROSS CEMENT RESTRICTOR— 510(k) K032095

Name: FDA 510(k) clearance K032095
Creator: U.S. Food and Drug Administration
Published: 2003-08-08

Substantially Equivalent

Interpore Cross Intl.

FDA 510(k) clearance K032095 for INTERPORE CROSS CEMENT RESTRICTOR, Substantially Equivalent on 2003-08-08. Applicant: Interpore Cross Intl.. Device class: 2.

Clearance details

Applicant: Interpore Cross Intl.
Product code: Code JDK
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 2003-07-08
Decision date: 2003-08-08
Decision: Substantially Equivalent
Clearance type: Special
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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