NUVASIVE CEMENT RESTRICTOR— 510(k) K032180

Unknown

Nuvasive, Inc.

FDA 510(k) clearance K032180 for NUVASIVE CEMENT RESTRICTOR, Unknown on 2003-10-07. Applicant: Nuvasive, Inc.. Device class: 2.

Clearance details

Applicant: Nuvasive, Inc.
Product code: Code JDK
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 2003-07-17
Decision date: 2003-10-07
Decision: Unknown
Clearance type: Traditional
Location: San Diego, 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.