FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
VKS/TC-PLUS REVISION KNEE
K Number: K032215
·
Decision Aug 8, 2003
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
38
Review Days
18
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Basic Information
- Device Name
- VKS/TC-PLUS REVISION KNEE
- K Number
- K032215
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 888.3560
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Plus Orthopedics
- Date Received
- July 21, 2003
- Decision Date
- August 8, 2003
- 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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Other Clearances by Plus Orthopedics
| K Number | Device Name | ||
|---|---|---|---|
| K032126 | PROMOS SHOULDER | Jan 8, 2004 | Substantially Equivalent |
| K033763 | MODIFICATION TO SLIM GLIDING NAIL SYSTEM | Dec 18, 2003 | Substantially Equivalent |
| K032709 | MODULAR PLUS HIP STEM | Sep 23, 2003 | Substantially Equivalent |
| K032548 | IP-XS COMPRESSION NAIL SYSTEM | Sep 10, 2003 | Substantially Equivalent |
| K032052 | UC-PLUS SOLUTION UNICONDYLAR KNEE | Jul 25, 2003 | Substantially Equivalent |
| K031165 | PLUS ORTHOPEDICS CEMENTED HIP STEM | Jun 6, 2003 | Substantially Equivalent |
| K030971 | MODIFICATION TO MODULAR PLUS REVISION STEM | Apr 24, 2003 | Substantially Equivalent |
| K024134 | UNI HIP STEM | Jan 15, 2003 | Substantially Equivalent |
| K023667 | RT-PLUS SOLUTION & RT-PLUS MODULAR SOLUTION KNEE | Dec 24, 2002 | Substantially Equivalent |
| K023416 | MODIFICATION TO VKS KNEE SYSTEM | Nov 8, 2002 | Substantially Equivalent |