Product code JDI— Orthopedic

PERFECTA TOTAL HIP SYSTEM

Classification name
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
Device class
Class 2
Regulation
21 CFR 888.3350
Advisory panel
Orthopedic
Total cleared
564
First cleared
Most recent

Market context for product code JDI

FDA has cleared 564 devices under product code JDI between 1977 and 2026, filed by 116 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 JDI

Adverse events under product code JDI

product code JDI
Death
65
Injury
12,943
Malfunction
1,681
Total
14,689

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 JDI

1–100 of 564

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