FDA product code QPP

Implantable Post-Surgical Kinematic Measurement Knee Device

Orthopedic·Class 2·21 CFR 888.3600·Implantable
US regulatory classifications
US Product Code (FDA)
QPP
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US Risk Class (FDA)
Class 2
US Regulation (CFR)
21 CFR 888.3600
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Medical specialty
Orthopedic
Device characteristics
GMP exempt
No
Implantable
Yes
Life-sustaining
No
Third party review
Not Eligible
Definition

An implantable post-surgical kinematic measurement knee device is a device that provides objective kinematic data after total knee arthroplasty surgery. The kinematic data provided by the device are used as an adjunct to other physiological parameter measurement tools utilized during the course of patient monitoring and treatment post-surgery.

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About this record

Implantable Post-Surgical Kinematic Measurement Knee Device is a medical device type in the Orthopedic specialty. This page includes real-world medical device registration data worldwide for this device type, with registrations from US FDA, Brazil ANVISA, and other global markets. This device type includes implantable products.

View regulatory classifications, recent 510(k) clearances, active device registrations, and similar products registered globally under this device category. Pure Global AI's free directory provides comprehensive worldwide registration intelligence across 7,000+ medical device types and 21 specialties.