VERASENSE Knee System— 510(k) K150372

Substantially Equivalent

Orthosensor, Inc.

FDA 510(k) clearance K150372 for VERASENSE Knee System, Substantially Equivalent on 2016-04-15. Applicant: Orthosensor, Inc..

Clearance details

Applicant: Orthosensor, Inc.
Product code: Code ONN
Advisory panel: Neurology
Date received: 2015-02-13
Decision date: 2016-04-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dania Beach, FL, US

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