OPTIMESH 500E CEMENT RESTRICTOR— 510(k) K033953

Unknown

Spineology, Inc.

FDA 510(k) clearance K033953 for OPTIMESH 500E CEMENT RESTRICTOR, Unknown on 2004-07-06. Applicant: Spineology, Inc.. Device class: 2.

Clearance details

Applicant: Spineology, Inc.
Product code: Code JDK
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 2003-12-22
Decision date: 2004-07-06
Decision: Unknown
Clearance type: Traditional
Location: Stillwater, MN, 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.