FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MIDASVu
K Number: K243020
·
Decision Dec 2, 2024
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
2
Review Days
66
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Basic Information
- Device Name
- MIDASVu
- K Number
- K243020
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.1100
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Intravu, Inc.
- Date Received
- September 27, 2024
- Decision Date
- December 2, 2024
- Product Code
- HRX
- 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 |
|---|---|---|---|
| HRX | Arthroscope | FDA class 2 | Orthopedic |
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Other Clearances by Intravu, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K181982 | MIDAScope and Introducer Kit, and MIDASystem | Aug 21, 2018 | Substantially Equivalent |