PIEZOSURGERY 3; OSSTEM PIEZO— 510(k) K091227
Substantially EquivalentPiezosurgery S.R.L.
FDA 510(k) clearance K091227 for PIEZOSURGERY 3; OSSTEM PIEZO, Substantially Equivalent on 2009-12-29. Applicant: Piezosurgery S.R.L.. Device class: 2.
Clearance details
- Applicant
- Piezosurgery S.R.L.
- 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
- Brescia, IT
Recent devices under product code DZI
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