KRQ — Prosthesis, Knee, Patello/Femorotibial, Constrained, Cemented, Polymer/Metal/Polymer Class II

FDA Device Classification

FDA product code KRQ covers "Prosthesis, Knee, Patello/Femorotibial, Constrained, Cemented, Polymer/Metal/Polymer", a Class II medical device regulated under 21 CFR 888.3550. Submissions are reviewed by the Orthopedic panel. Devices under this code are implants.

Classification Details

Product Code
KRQ
Device Class
Class II
Regulation Number
888.3550
Submission Type
Review Panel
OR
Medical Specialty
Orthopedic
Implant
Yes