FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇪 Germany
ACRIFIX
K Number: K230341
·
Decision Apr 6, 2023
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
329
Applicant Total
6
Review Days
57
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Basic Information
- Device Name
- ACRIFIX
- K Number
- K230341
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3760
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Deltamed GmbH
- Date Received
- February 8, 2023
- Decision Date
- April 6, 2023
- 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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Other Clearances by Deltamed GmbH
| K Number | Device Name | ||
|---|---|---|---|
| K243720 | 3Delta UNlimited | Dec 18, 2024 | Substantially Equivalent |
| K212541 | 3Delta Denture Base - 3Delta Denture Bond - 3Delta Denture Fix | Jan 10, 2022 | Substantially Equivalent |
| K211804 | 3Delta Crown | Dec 6, 2021 | Substantially Equivalent |
| K200039 | P pro Crown & Bridge | Jul 31, 2020 | Substantially Equivalent |
| K102776 | EXTRA-ORAL, ADDITIVE COMPUTER AIDED MANUFACTURE AND CURING SYSTEM | Feb 18, 2011 | Substantially Equivalent |