FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
RT-PLUS MODULAR CEMENTED KNEE COMPONENTS
K Number: K003504
·
Decision May 11, 2001
Classifications
1
FEI Numbers
140
Registration Numbers
140
Same Product Code
82
Applicant Total
38
Review Days
179
Basic Information
- Device Name
- RT-PLUS MODULAR CEMENTED KNEE COMPONENTS
- K Number
- K003504
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3510
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- PLUS ORTHOPEDICS
- Date Received
- November 13, 2000
- Decision Date
- May 11, 2001
- Product Code
- KRO
- 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 |
|---|---|---|---|
| KRO | Prosthesis, Knee, Femorotibial, Constrained, Cemented, 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 |
| K032215 | VKS/TC-PLUS REVISION KNEE | Aug 8, 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 |