IN-CERAM SPINELL— 510(k) K951183
Substantially EquivalentVident
FDA 510(k) clearance K951183 for IN-CERAM SPINELL, Substantially Equivalent on 1995-05-02. Applicant: Vident. Device class: 2.
Clearance details
- Applicant
- Vident
- Product code
- Code EIH
- Device class
- Class 2
- Regulation
- 21 CFR 872.6660
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Baldwin Park, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.