FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
JOURNEY II UK and ENGAGE Cementless Partial Knee System
K Number: K222653
·
Decision Oct 28, 2022
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
4
Applicant Total
1
Review Days
57
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Basic Information
- Device Name
- JOURNEY II UK and ENGAGE Cementless Partial Knee System
- K Number
- K222653
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3535
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Smith+Nephew, Inc.
- Date Received
- September 1, 2022
- Decision Date
- October 28, 2022
- Product Code
- NJD
- 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 |
|---|---|---|---|
| NJD | Prosthesis, Knee, Femorotibial, Unicompartmental/Unicondylar, Uncemented, Porous-Coated, Metal/Polymer | FDA class 2 | Orthopedic |
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