FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Voyant System
K Number: K191579
·
Decision Jul 11, 2019
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
2
Review Days
27
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Basic Information
- Device Name
- Voyant System
- K Number
- K191579
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 888.1100
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Viseon, Inc.
- Date Received
- June 14, 2019
- Decision Date
- July 11, 2019
- Product Code
- HRX
- Advisory Committee
- Orthopedic
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| HRX | Arthroscope | FDA class 2 | Orthopedic |
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Other Clearances by Viseon, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K181885 | Voyant System | Oct 2, 2018 | Substantially Equivalent |