NUVASIVE PERCUTANEOUS TRANSFACET/INTRAPEDICULAR SCREW— 510(k) K001323

Name: FDA 510(k) clearance K001323
Creator: U.S. Food and Drug Administration
Published: 2000-07-25

Substantially Equivalent

Nuvasive, Inc.

FDA 510(k) clearance K001323 for NUVASIVE PERCUTANEOUS TRANSFACET/INTRAPEDICULAR SCREW, Substantially Equivalent on 2000-07-25. Applicant: Nuvasive, Inc.. Device class: Unclassified.

Clearance details

Applicant: Nuvasive, Inc.
Product code: Code MRW
Device class: Unclassified
Advisory panel: Unknown
Date received: 2000-04-26
Decision date: 2000-07-25
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.