FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇱 Israel
XACT Robotic System
K Number: K191332
·
Decision Oct 3, 2019
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
818
Applicant Total
4
Review Days
140
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Basic Information
- Device Name
- XACT Robotic System
- K Number
- K191332
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1750
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Xact Robotics, Ltd.
- Date Received
- May 16, 2019
- Decision Date
- October 3, 2019
- Product Code
- JAK
- Advisory Committee
- Radiology
- Review Advisory Committee
- RA
- 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 |
|---|---|---|---|
| JAK | System, X-Ray, Tomography, Computed | FDA class 2 | Radiology |
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