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
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JWH), ordered by most recent decision date.

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Other Clearances by Plus Orthopedics

K Number Device Name
K032126 PROMOS SHOULDER
K033763 MODIFICATION TO SLIM GLIDING NAIL SYSTEM
K032709 MODULAR PLUS HIP STEM
K032548 IP-XS COMPRESSION NAIL SYSTEM
K032052 UC-PLUS SOLUTION UNICONDYLAR KNEE
K031165 PLUS ORTHOPEDICS CEMENTED HIP STEM
K030971 MODIFICATION TO MODULAR PLUS REVISION STEM
K024134 UNI HIP STEM
K023667 RT-PLUS SOLUTION & RT-PLUS MODULAR SOLUTION KNEE
K023416 MODIFICATION TO VKS KNEE SYSTEM
Search all 38 clearances from Plus Orthopedics →