FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Vericore Gradient Temporary Disc
K Number: K152443
·
Decision May 11, 2016
Classifications
1
FEI Numbers
180
Registration Numbers
180
Same Product Code
188
Applicant Total
4
Review Days
258
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Basic Information
- Device Name
- Vericore Gradient Temporary Disc
- K Number
- K152443
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3770
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Whip Mix Corporation
- Date Received
- August 27, 2015
- Decision Date
- May 11, 2016
- Product Code
- EBG
- 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 |
|---|---|---|---|
| EBG | Crown And Bridge, Temporary, Resin | FDA class 2 | Dental |
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