DeviceClearance

Product code JDS— Orthopedic

KNEE FUSION NAIL

Classification name
Nail, Fixation, Bone
Device class
Class 2
Regulation
21 CFR 888.3030
Advisory panel
Orthopedic
Total cleared
53
First cleared
Most recent

Market context for product code JDS

FDA has cleared 53 devices under product code JDS between 1977 and 2025, filed by 26 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 JDS

Adverse events under product code JDS

product code JDS
Injury
1,776
Malfunction
1,509
Total
3,285

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 JDS

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