510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K080437Substantially Equivalent

Micrus Microcoil System, Deltapaq 10 Cerecyte, Model Cdf

Micrus Endovascular Corporation, San Jose CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K080437 is the FDA 510(k) clearance record for MICRUS MICROCOIL SYSTEM, DELTAPAQ 10 CERECYTE, MODEL CDF, a class II device, cleared for Micrus Endovascular Corporation on under FDA product code HCG (Device, Neurovascular Embolization). FDA records list 23 510(k) clearances for Micrus Endovascular Corporation, from to . As of , FDA records show no recalls naming K080437.

Clearance record

Decision date
Received
(83 days to decision)
Product code
HCG Device, Neurovascular Embolization
Regulation
21 CFR 882.5950
Device class
Class II
Review panel
Neurology
Applicant
Micrus Endovascular Corporation 821 Fox Ln., San Jose CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HCG

Trailing 12 months
5 clearances under product code HCG in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HCG, trailing twelve months
MonthClearances
November 20250
December 20251
January 20261
February 20260
March 20260
April 20260
May 20261
June 20261
July 20260
August 20261
September 20260
October 20260