FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Porous Patella and Porous Tibia Baseplate
K Number: K211221
·
Decision Oct 1, 2021
Classifications
1
FEI Numbers
219
Registration Numbers
219
Same Product Code
133
Applicant Total
83
Review Days
161
Basic Information
- Device Name
- Porous Patella and Porous Tibia Baseplate
- K Number
- K211221
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3565
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Smith & Nephew, Inc.
- Date Received
- April 23, 2021
- Decision Date
- October 1, 2021
- Product Code
- MBH
- 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 |
|---|---|---|---|
| MBH | Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer | FDA class 2 | Orthopedic |
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