FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇭 Switzerland
MySpine S2-Alar/Alar-Iliac Pedicle Screw Placement Guides
K Number: K200792
·
Decision Oct 5, 2020
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
7
Applicant Total
4
Review Days
193
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Basic Information
- Device Name
- MySpine S2-Alar/Alar-Iliac Pedicle Screw Placement Guides
- K Number
- K200792
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3070
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Medacta Inernational SA
- Date Received
- March 26, 2020
- Decision Date
- October 5, 2020
- Product Code
- PQC
- 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 |
|---|---|---|---|
| PQC | Pedicle Screw Placement Guide | FDA class 2 | Orthopedic |
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