Typhoon(TM) Facet Screw Fixation System— 510(k) K121850

Name: FDA 510(k) clearance K121850
Creator: U.S. Food and Drug Administration
Published: 2012-09-20

Substantially Equivalent

Choicespine, LP

FDA 510(k) clearance K121850 for Typhoon(TM) Facet Screw Fixation System, Substantially Equivalent on 2012-09-20. Applicant: Choicespine, LP. Device class: Unclassified.

Clearance details

Applicant: Choicespine, LP
Product code: Code MRW
Device class: Unclassified
Advisory panel: Unknown
Date received: 2012-06-25
Decision date: 2012-09-20
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.