OSTEON III— 510(k) K153676
Substantially EquivalentGenoss Co., Ltd.
FDA 510(k) clearance K153676 for OSTEON III, Substantially Equivalent on 2016-09-14. Applicant: Genoss Co., Ltd..
Clearance details
- Applicant
- Genoss Co., Ltd.
- Product code
- Code LYC
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Suwon-Si, KR
Data sourced from openFDA. This site is unofficial and independent of the FDA.