Piezosurgery White— 510(k) K171326
Substantially EquivalentMectron S.P.A.
FDA 510(k) clearance K171326 for Piezosurgery White, Substantially Equivalent on 2018-04-13. Applicant: Mectron S.P.A.. Device class: 2.
Clearance details
- Applicant
- Mectron S.P.A.
- Product code
- Code DZI
- Device class
- Class 2
- Regulation
- 21 CFR 872.4120
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Carasco, IT
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