PEDIGUARD NERVE DETECTOR SYSTEM— 510(k) K123390

Substantially Equivalent

Spineguard S.A.

FDA 510(k) clearance K123390 for PEDIGUARD NERVE DETECTOR SYSTEM, Substantially Equivalent on 2013-08-08. Applicant: Spineguard S.A..

Clearance details

Applicant: Spineguard S.A.
Product code: Code PDQ
Advisory panel: Ear, Nose, Throat
Date received: 2012-11-02
Decision date: 2013-08-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

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