Product code ITW— Physical Medicine

ANKLE FOOT ORTHOSIS

Classification name
Joint, Ankle, External Brace
Device class
Class 1
Regulation
21 CFR 890.3475
Advisory panel
Physical Medicine
Total cleared
1
First cleared
Most recent

Market context for product code ITW

FDA has cleared 1 device under product code ITW, all in 1982, filed by 1 applicant company. 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.

Top applicants under product code ITW

Recent clearances under product code ITW

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