FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CERADIUM V NON-PRECIOUS CERAMIC ALLOY
K Number: K993572
·
Decision Dec 13, 1999
Classifications
1
FEI Numbers
94
Registration Numbers
94
Same Product Code
152
Applicant Total
6
Review Days
53
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Basic Information
- Device Name
- CERADIUM V NON-PRECIOUS CERAMIC ALLOY
- K Number
- K993572
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3710
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Matech, Inc.
- Date Received
- October 21, 1999
- Decision Date
- December 13, 1999
- Product Code
- EJH
- 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 |
|---|---|---|---|
| EJH | Alloy, Metal, Base | FDA class 2 | Dental |
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Other Clearances by Matech, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K010069 | DURABOND NON-PRECIOUS CERAMIC ALLOY | Feb 15, 2001 | Substantially Equivalent |
| K992881 | HI BOND NON-PRECIOUS CERAMIC ALLOY | Nov 19, 1999 | Substantially Equivalent |
| K992705 | CERADIUM NON-PRECIOUS CERAMIC ALLOY | Sep 22, 1999 | Substantially Equivalent |
| K974894 | KROMATICA COLOR CHANGING ALGINATE | Feb 12, 1998 | Substantially Equivalent |
| K925746 | REPLICA | Jan 21, 1994 | Substantially Equivalent |