KMI CEMENT RESTRICTOR IMPLANT— 510(k) K061465

Unknown

Kinetikos Medical, Inc.

FDA 510(k) clearance K061465 for KMI CEMENT RESTRICTOR IMPLANT, Unknown on 2006-10-05. Applicant: Kinetikos Medical, Inc.. Device class: 2.

Clearance details

Applicant: Kinetikos Medical, Inc.
Product code: Code JDK
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 2006-05-26
Decision date: 2006-10-05
Decision: Unknown
Clearance type: Traditional
Location: Carlsbad, CA, 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.