FDA 510(k)
FDA class 2
Substantially Equivalent
🇬🇧 United Kingdom
NEOSS VARIOUS TITANIUM ABUTMENTS
K Number: K071838
·
Decision Oct 19, 2007
Classifications
1
FEI Numbers
390
Registration Numbers
390
Same Product Code
672
Applicant Total
4
Review Days
106
Basic Information
- Device Name
- NEOSS VARIOUS TITANIUM ABUTMENTS
- K Number
- K071838
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3630
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- NEOSS LTD
- Date Received
- July 5, 2007
- Decision Date
- October 19, 2007
- 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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