FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇭 Switzerland
Straumann TLX Variobase C
K Number: K220878
·
Decision Jun 16, 2022
Classifications
1
FEI Numbers
390
Registration Numbers
390
Same Product Code
672
Applicant Total
49
Review Days
83
Basic Information
- Device Name
- Straumann TLX Variobase C
- K Number
- K220878
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3630
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Institut Straumann AG
- Date Received
- March 25, 2022
- Decision Date
- June 16, 2022
- 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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