FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
RETROMTA-ORTHOMTA II
K Number: K132825
·
Decision Apr 10, 2014
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
142
Applicant Total
1
Review Days
213
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Basic Information
- Device Name
- RETROMTA-ORTHOMTA II
- K Number
- K132825
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3820
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Biomta
- Date Received
- September 9, 2013
- Decision Date
- April 10, 2014
- Product Code
- KIF
- 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 |
|---|---|---|---|
| KIF | Resin, Root Canal Filling | FDA class 2 | Dental |
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