Product code HAO— Neurology

AUTO SUTURE PITUITARY SPINAL RONGEUR

Classification name
Instrument, Surgical, Non-Powered
Device class
Class 1
Regulation
21 CFR 882.4535
Advisory panel
Neurology
Total cleared
34
First cleared
Most recent

Market context for product code HAO

FDA has cleared 34 devices under product code HAO between 1976 and 2022, filed by 18 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 HAO

Recent clearances under product code HAO

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