FDA 510(k)
FDA class 2
Substantially Equivalent
🇱🇮 Liechtenstein
IPS e.max CAD Abutment Solutions- extra systems
K Number: K191382
·
Decision Aug 26, 2019
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
31
Review Days
95
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Basic Information
- Device Name
- IPS e.max CAD Abutment Solutions- extra systems
- K Number
- K191382
- Device Class
- FDA class 2
- Clearance Type
- Abbreviated
- Regulation Number
- 872.3630
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Ivoclar Vivadent, AG
- Date Received
- May 23, 2019
- Decision Date
- August 26, 2019
- Product Code
- NHA
- 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 |
|---|---|---|---|
| NHA | Abutment, Implant, Dental, Endosseous | FDA class 2 | Dental |
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