SURGYBONE— 510(k) K083569
Substantially EquivalentSilfradent S.R.L.
FDA 510(k) clearance K083569 for SURGYBONE, Substantially Equivalent on 2009-04-01. Applicant: Silfradent S.R.L.. Device class: 2.
Clearance details
- Applicant
- Silfradent 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
- Abbreviated
- Location
- Ormond Beach, FL, US
Recent devices under product code DZI
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