NUVASIVE TRIAD FACET SCREW SYSTEM— 510(k) K020411

Name: FDA 510(k) clearance K020411
Creator: U.S. Food and Drug Administration
Published: 2002-03-12

Substantially Equivalent

Nuvasive, Inc.

FDA 510(k) clearance K020411 for NUVASIVE TRIAD FACET SCREW SYSTEM, Substantially Equivalent on 2002-03-12. Applicant: Nuvasive, Inc.. Device class: Unclassified.

Clearance details

Applicant: Nuvasive, Inc.
Product code: Code MRW
Device class: Unclassified
Advisory panel: Unknown
Date received: 2002-02-07
Decision date: 2002-03-12
Decision: Substantially Equivalent
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.