FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇭 Switzerland
Trabis
K Number: K173893
·
Decision Sep 6, 2018
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
17
Applicant Total
4
Review Days
259
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Basic Information
- Device Name
- Trabis
- K Number
- K173893
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3060
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Coligne AG
- Date Received
- December 21, 2017
- Decision Date
- September 6, 2018
- Product Code
- PLR
- Advisory Committee
- Orthopedic
- Review Advisory Committee
- OR
- 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 |
|---|---|---|---|
| PLR | Spinal Vertebral Body Replacement Device - Cervical | FDA class 2 | Orthopedic |
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