FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇭 Switzerland
MySpine Pedicle Screw Placement Guides - LP
K Number: K153273
·
Decision Jun 29, 2016
Classifications
1
FEI Numbers
354
Registration Numbers
354
Same Product Code
302
Applicant Total
87
Review Days
230
Basic Information
- Device Name
- MySpine Pedicle Screw Placement Guides - LP
- K Number
- K153273
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3070
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Medacta International SA
- Date Received
- November 12, 2015
- Decision Date
- June 29, 2016
- Product Code
- MNI
- 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 |
|---|---|---|---|
| MNI | Orthosis, Spinal Pedicle Fixation | FDA class 2 | Orthopedic |
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