BONART MODEL ART-IM1 IMPLANTOR SYSTEM & ACCESSORIES— 510(k) K100785
Substantially EquivalentBonart Co., Ltd.
FDA 510(k) clearance K100785 for BONART MODEL ART-IM1 IMPLANTOR SYSTEM & ACCESSORIES, Substantially Equivalent on 2010-12-03. Applicant: Bonart Co., Ltd.. Device class: 1.
Clearance details
- Applicant
- Bonart Co., Ltd.
- Product code
- Code EBW
- Device class
- Class 1
- Regulation
- 21 CFR 872.4200
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walnut, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.