FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BONE-LOCK
K Number: K954030
·
Decision Nov 14, 1997
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
3
Review Days
809
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Basic Information
- Device Name
- BONE-LOCK
- K Number
- K954030
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3640
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Leibinger GmbH
- Date Received
- August 28, 1995
- Decision Date
- November 14, 1997
- Product Code
- DZE
- 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 |
|---|---|---|---|
| DZE | Implant, Endosseous, Root-Form | FDA class 2 | Dental |
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