MICROPLEX COIL SYSTEM (MCS) AND HYDROCOIL EMBOLIC SYSTEM (HES)— 510(k) K050954

Substantially Equivalent

MicroVention, Inc.

FDA 510(k) clearance K050954 for MICROPLEX COIL SYSTEM (MCS) AND HYDROCOIL EMBOLIC SYSTEM (HES), Substantially Equivalent on 2005-06-28. Applicant: MicroVention, Inc.. Device class: 2.

Clearance details

Applicant
MicroVention, Inc.
Product code
Code HCG
Device class
Class 2
Regulation
21 CFR 882.5950
Advisory panel
Neurology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Aliso Viejo, CA, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code HCG

product code HCG
Death
50
Injury
801
Malfunction
5,625
Total
6,476

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 K050954

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 K050954.

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