Last synced on 18 April 2025 at 11:05 pm

Knee Arthroplasty Implantation System

Page Type
Product Code
Definition
Intended to be used to assist in the implantation of a specific knee arthroplasty device or a set of specific knee arthroplasty devices. Indicated to include guiding alignment, making or establishing cuts, selecting, sizing, attaching, positioning or orienting implant components.
Physical State
A device accessory or set of device accessories;
Technical Method
Aids the surgeon in performing the implantation of the knee implant
Target Area
Knee
Regulation Medical Specialty
Orthopedic
Review Panel
Orthopedic
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
888.3560
GMP Exempt?
No
Summary Malfunction Reporting
Eligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

CFR § 888.3560 Knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis

§ 888.3560 Knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis.

(a) Identification. A knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis is a device intended to be implanted to replace a knee joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. This generic type of device includes prostheses that have a femoral component made of alloys, such as cobalt-chromium-molybdenum, and a tibial component or components and a retropatellar resurfacing component made of ultra-high molecular weight polyethylene. This generic type of device is limited to those prostheses intended for use with bone cement (§ 888.3027).

(b) Classification. Class II.

Knee Arthroplasty Implantation System

Page Type
Product Code
Definition
Intended to be used to assist in the implantation of a specific knee arthroplasty device or a set of specific knee arthroplasty devices. Indicated to include guiding alignment, making or establishing cuts, selecting, sizing, attaching, positioning or orienting implant components.
Physical State
A device accessory or set of device accessories;
Technical Method
Aids the surgeon in performing the implantation of the knee implant
Target Area
Knee
Regulation Medical Specialty
Orthopedic
Review Panel
Orthopedic
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
888.3560
GMP Exempt?
No
Summary Malfunction Reporting
Eligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

CFR § 888.3560 Knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis

§ 888.3560 Knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis.

(a) Identification. A knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis is a device intended to be implanted to replace a knee joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. This generic type of device includes prostheses that have a femoral component made of alloys, such as cobalt-chromium-molybdenum, and a tibial component or components and a retropatellar resurfacing component made of ultra-high molecular weight polyethylene. This generic type of device is limited to those prostheses intended for use with bone cement (§ 888.3027).

(b) Classification. Class II.