DeviceClearance

Product code JDO— Orthopedic

CONQUEST FN

Classification name
Device, Fixation, Proximal Femoral, Implant
Device class
Class 2
Regulation
21 CFR 888.3030
Advisory panel
Orthopedic
Total cleared
23
First cleared
Most recent

Market context for product code JDO

FDA has cleared 23 devices under product code JDO between 1978 and 2023, filed by 12 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

last 15 years

Top applicants under product code JDO

Recent clearances under product code JDO

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