DeviceClearance

Product code KRD— Cardiovascular

INTERLOCK-35 FIBERED IDC OCCLUSION SYSTEM

Classification name
Device, Vascular, For Promoting Embolization
Device class
Class 2
Regulation
21 CFR 870.3300
Advisory panel
Cardiovascular
Total cleared
132
First cleared
Most recent

Market context for product code KRD

FDA has cleared 132 devices under product code KRD between 1985 and 2026, filed by 53 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 KRD

Adverse events under product code KRD

product code KRD
Death
119
Injury
1,869
Malfunction
7,015
Other
1
Total
9,004

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 KRD

1–100 of 132

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