FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ArgenIS Titanium Abutments
K Number: K160248
·
Decision Aug 5, 2016
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
5
Review Days
186
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Basic Information
- Device Name
- ArgenIS Titanium Abutments
- K Number
- K160248
- Device Class
- FDA class 2
- Clearance Type
- Abbreviated
- Regulation Number
- 872.3630
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Argen Corporation
- Date Received
- February 1, 2016
- Decision Date
- August 5, 2016
- 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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