INTERPORE CROSS CEMENT RESTRICTOR— 510(k) K023908

Unknown

Interpore Cross Intl.

FDA 510(k) clearance K023908 for INTERPORE CROSS CEMENT RESTRICTOR, Unknown on 2003-05-16. 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: 2002-11-25
Decision date: 2003-05-16
Decision: Unknown
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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K042798 — C-TEK C-TRUN ANTERIOR CERVICAL PLATE SYSTEM2004-11-04

Data sourced from openFDA. This site is unofficial and independent of the FDA.