FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Ventris Intervertebral Body Fusion Device
K Number: K243386
·
Decision Apr 22, 2025
Classifications
1
FEI Numbers
254
Registration Numbers
254
Same Product Code
194
Applicant Total
1
Review Days
173
Basic Information
- Device Name
- Ventris Intervertebral Body Fusion Device
- K Number
- K243386
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3080
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Acuity Surgical Devices LLC
- Date Received
- October 31, 2024
- Decision Date
- April 22, 2025
- Product Code
- OVD
- 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 |
|---|---|---|---|
| OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | FDA class 2 | Orthopedic |
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