L300 Go System— 510(k) K162407

Substantially Equivalent

Bioness, Inc.

FDA 510(k) clearance K162407 for L300 Go System, Substantially Equivalent on 2017-01-27. Applicant: Bioness, Inc..

Clearance details

Applicant: Bioness, Inc.
Product code: Code GZI
Advisory panel: Neurology
Date received: 2016-08-29
Decision date: 2017-01-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Valencia, CA, US

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