PEDIGUARD NERVE DETECTOR SYSTEM— 510(k) K123390
Substantially EquivalentSpineguard S.A.
FDA 510(k) clearance K123390 for PEDIGUARD NERVE DETECTOR SYSTEM, Substantially Equivalent on 2013-08-08. Applicant: Spineguard S.A.. Device class: 2.
Clearance details
- Applicant
- Spineguard S.A.
- Product code
- Code PDQ
- Device class
- Class 2
- Regulation
- 21 CFR 874.1820
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
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More clearances from Spineguard S.A.
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