FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MOBIO Total Knee System Posterior Stabilized (PS and PS+) Tibial Inserts, MOBIO Total Knee System Patellar Component
K Number: K183025
·
Decision Jan 28, 2019
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
12
Review Days
88
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Basic Information
- Device Name
- MOBIO Total Knee System Posterior Stabilized (PS and PS+) Tibial Inserts, MOBIO Total Knee System Patellar Component
- K Number
- K183025
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3560
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- B-One Ortho, Corp.
- Date Received
- November 1, 2018
- Decision Date
- January 28, 2019
- Product Code
- JWH
- 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 |
|---|---|---|---|
| JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | FDA class 2 | Orthopedic |
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| K180446 | b-ONE Total Knee System | Oct 12, 2018 | Substantially Equivalent |