Choice Spine Laminoplasty Fixation System— 510(k) K173215

Name: FDA 510(k) clearance K173215
Creator: U.S. Food and Drug Administration
Published: 2018-01-19

Substantially Equivalent

Choicespine, LP

FDA 510(k) clearance K173215 for Choice Spine Laminoplasty Fixation System, Substantially Equivalent on 2018-01-19. Applicant: Choicespine, LP. Device class: 2.

Clearance details

Applicant: Choicespine, LP
Product code: Code NQW
Device class: Class 2
Regulation: 21 CFR 888.3050
Advisory panel: Orthopedic
Date received: 2017-10-02
Decision date: 2018-01-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Knoxville, TN, 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.