FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MODIFICATION TO: OSTEOGRAF/N-700
K Number: K072058
·
Decision Aug 3, 2007
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
229
Applicant Total
13
Review Days
8
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Basic Information
- Device Name
- MODIFICATION TO: OSTEOGRAF/N-700
- K Number
- K072058
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 872.3930
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Dentsply Interntional
- Date Received
- July 26, 2007
- Decision Date
- August 3, 2007
- Product Code
- LYC
- 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 |
|---|---|---|---|
| LYC | Bone Grafting Material, Synthetic | FDA class 2 | Dental |
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