FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MODUS TRILOCK 2.0/2.3/2.5
K Number: K071612
·
Decision Sep 11, 2007
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
291
Applicant Total
42
Review Days
90
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Basic Information
- Device Name
- MODUS TRILOCK 2.0/2.3/2.5
- K Number
- K071612
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.4760
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Medartis AG
- Date Received
- June 13, 2007
- Decision Date
- September 11, 2007
- Product Code
- JEY
- 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 |
|---|---|---|---|
| JEY | Plate, Bone | FDA class 2 | Dental |
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