FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ORTHO-KEV APPLIANCE REINFORCING SYSTEM
K Number: K895714
·
Decision Dec 21, 1989
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
329
Applicant Total
45
Review Days
87
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Basic Information
- Device Name
- ORTHO-KEV APPLIANCE REINFORCING SYSTEM
- K Number
- K895714
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3760
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Applicant
- American Orthodontics
- Date Received
- September 25, 1989
- Decision Date
- December 21, 1989
- Product Code
- EBI
- 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 |
|---|---|---|---|
| EBI | Resin, Denture, Relining, Repairing, Rebasing | FDA class 2 | Dental |
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