CENTERPULSE, SPINE-TECH DIVISION CEMENT RESTRICTOR— 510(k) K022615

Name: FDA 510(k) clearance K022615
Creator: U.S. Food and Drug Administration
Published: 2002-10-29

Unknown

Centerpulse Spine-Tech, Inc.

FDA 510(k) clearance K022615 for CENTERPULSE, SPINE-TECH DIVISION CEMENT RESTRICTOR, Unknown on 2002-10-29. Applicant: Centerpulse Spine-Tech, Inc.. Device class: 2.

Clearance details

Applicant: Centerpulse Spine-Tech, Inc.
Product code: Code JDK
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 2002-08-07
Decision date: 2002-10-29
Decision: Unknown
Clearance type: Special
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

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