Product code KNN— Physical Medicine

(ROTH)SPIRAL ROTATING PROSTATIC BIOPSY NEEDLE

Classification name
Components, Wheelchair
Device class
Class 1
Regulation
21 CFR 890.3920
Advisory panel
Physical Medicine
Total cleared
64
First cleared
Most recent

Market context for product code KNN

FDA has cleared 64 devices under product code KNN between 1977 and 2022, filed by 38 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Clearances per year

last 15 years

Top applicants under product code KNN

Recent clearances under product code KNN

Data sourced from openFDA. This site is unofficial and independent of the FDA.