ATRIUM ICAST COVERED STENT— 510(k) K050814

Substantially Equivalent

Atrium Medical Corp.

FDA 510(k) clearance K050814 for ATRIUM ICAST COVERED STENT, Substantially Equivalent on 2005-05-06. Applicant: Atrium Medical Corp.. Device class: 2.

Clearance details

Applicant
Atrium Medical Corp.
Product code
Code JCT
Device class
Class 2
Regulation
21 CFR 878.3720
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Hudson, NH, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code JCT

view all

More clearances from Atrium Medical Corp.

view all

Adverse events under product code JCT

product code JCT
Death
20
Injury
211
Other
1
Total
232

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 →

Recalls naming K050814

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K050814.

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