VSTAAR AdjusteR— 510(k) K160278

Name: FDA 510(k) clearance K160278
Creator: U.S. Food and Drug Administration
Published: 2016-11-04

Substantially Equivalent

Spinal Acoustics, LLC

FDA 510(k) clearance K160278 for VSTAAR AdjusteR, Substantially Equivalent on 2016-11-04. Applicant: Spinal Acoustics, LLC. Device class: Unclassified.

Clearance details

Applicant: Spinal Acoustics, LLC
Product code: Code LXM
Device class: Unclassified
Advisory panel: Unknown
Date received: 2016-02-02
Decision date: 2016-11-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Beaver, PA, US

Download summary PDF View on FDA.gov ↗

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