NuVasive® VersaTie System— 510(k) K173117

Substantially Equivalent

Nuvasive, Inc.

FDA 510(k) clearance K173117 for NuVasive® VersaTie System, Substantially Equivalent on 2017-12-07. Applicant: Nuvasive, Inc.. Device class: 2.

Clearance details

Applicant: Nuvasive, Inc.
Product code: Code OWI
Device class: Class 2
Regulation: 21 CFR 888.3010
Advisory panel: Orthopedic
Date received: 2017-09-29
Decision date: 2017-12-07
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.