Hoggan Scientific® microFET2— 510(k) K162412

Name: FDA 510(k) clearance K162412
Creator: U.S. Food and Drug Administration
Published: 2017-03-09

Substantially Equivalent

Hoggan Scientific, LLC

FDA 510(k) clearance K162412 for Hoggan Scientific® microFET2, Substantially Equivalent on 2017-03-09. Applicant: Hoggan Scientific, LLC. Device class: 2.

Clearance details

Applicant: Hoggan Scientific, LLC
Product code: Code LBB
Device class: Class 2
Regulation: 21 CFR 888.1240
Advisory panel: Orthopedic
Date received: 2016-08-29
Decision date: 2017-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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