FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DuraPro Oscillating System
K Number: K240568
·
Decision Apr 29, 2024
Classifications
1
FEI Numbers
370
Registration Numbers
370
Same Product Code
404
Applicant Total
11
Review Days
60
Basic Information
- Device Name
- DuraPro Oscillating System
- K Number
- K240568
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.4560
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Globus Medical, Inc.
- Date Received
- February 29, 2024
- Decision Date
- April 29, 2024
- Product Code
- OLO
- Advisory Committee
- Neurology
- 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 |
|---|---|---|---|
| OLO | Orthopedic Stereotaxic Instrument | FDA class 2 | Neurology |
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