Product code HST— Orthopedic

OCTAGONAL ALUMINUM FRAMING SYSTEM

Classification name
Apparatus, Traction, Non-Powered
Device class
Class 1
Regulation
21 CFR 888.5850
Advisory panel
Orthopedic
Total cleared
38
First cleared
Most recent

Market context for product code HST

FDA has cleared 38 devices under product code HST between 1977 and 2016, filed by 27 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

Top applicants under product code HST

Adverse events under product code HST

product code HST
Other
1
Total
1

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recent clearances under product code HST

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