FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Locator Overdenture Implant System
K Number: K203701
·
Decision Apr 15, 2021
Classifications
1
FEI Numbers
333
Registration Numbers
333
Same Product Code
1516
Applicant Total
1
Review Days
118
Basic Information
- Device Name
- Locator Overdenture Implant System
- K Number
- K203701
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3640
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Ivory Super Holdco Inc. / Zest Anchors LLC
- Date Received
- December 18, 2020
- Decision Date
- April 15, 2021
- Product Code
- DZE
- Advisory Committee
- Dental
- Review Advisory Committee
- DE
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| DZE | Implant, Endosseous, Root-Form | FDA class 2 | Dental |
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