Medical Devices; Orthopedic Devices; Classification of the Implantable Post-Surgical Kinematic Measurement Knee Device
fda-device · Food and Drug Administration · Rule · Published 2023-01-05 · Effective 2023-01-05 · 88 FR 751
Document
Document number
2022-28604
Federal Register citation
88 FR 751
CFR reference
21 CFR 888
Type
Rule
Action
Final amendment; final order.
Category
fda-device
Sub-agency
Food and Drug Administration
Publication date
2023-01-05
Effective date
2023-01-05
HHS docket
Docket No. FDA-2022-N-3239
Abstract
The Food and Drug Administration (FDA, Agency or we) is classifying the implantable post-surgical kinematic measurement knee device into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for the implantable post-surgical kinematic measurement knee device's classification. We are taking this action because we have determined that classifying the device into class II (special controls) will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices.