FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
VERICORE ABUTMENT IN ZIRCONIA FOR IMPLANT SYSTEMS
K Number: K090976
·
Decision Jun 25, 2009
Classifications
1
FEI Numbers
390
Registration Numbers
390
Same Product Code
672
Applicant Total
4
Review Days
80
Basic Information
- Device Name
- VERICORE ABUTMENT IN ZIRCONIA FOR IMPLANT SYSTEMS
- K Number
- K090976
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3630
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- WHIP-MIX CORP.
- Date Received
- April 6, 2009
- Decision Date
- June 25, 2009
- 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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