FDA 510(k)
FDA class 2
Substantially Equivalent
🇧🇪 Belgium
Wishbone HA
K Number: K211551
·
Decision Aug 20, 2021
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
39
Applicant Total
1
Review Days
93
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Basic Information
- Device Name
- Wishbone HA
- K Number
- K211551
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3930
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Wishbone SA
- Date Received
- May 19, 2021
- Decision Date
- August 20, 2021
- Product Code
- NPM
- 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 |
|---|---|---|---|
| NPM | Bone Grafting Material, Animal Source | FDA class 2 | Dental |
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