510(K) CLEARANCES 49 ▼18RECALLS POSTED 23 ▼3CLASS I 1 ▼1PMA DECISIONS 37 ▼3WEEK ENDING / FDA DATA AS OF
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K111010Substantially Equivalent

Spiderfx Embolic Protection Device

Medtronic, Inc., Plymouth MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K111010 is the FDA 510(k) clearance record for SPIDERFX EMBOLIC PROTECTION DEVICE, a class II device, cleared for Ev3, Inc. on under FDA product code NTE (Temporary Carotid Catheter For Embolic Capture). FDA's definition for product code NTE reads: "This device is a single use percutaneous catheter system that is introduced into an artery through the skin using a guidewire. The catheter has an embolic capture filter or an occlusion balloon at the distal end. The filter or balloon can...". FDA records list 1,525 510(k) clearances for Medtronic, Inc., from to . As of , FDA records show no recalls naming K111010.

Clearance record

Decision date
Received
(199 days to decision)
Product code
NTE Temporary Carotid Catheter For Embolic Capture
Regulation
21 CFR 870.1250
Device class
Class II
Review panel
Cardiovascular
Applicant
Ev3, Inc. 3033 Campus Dr., Plymouth MN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NTE

Trailing 12 months

FDA records hold no clearances under product code NTE in the trailing twelve months.

FDA records show no clearances under product code NTE in the twelve months to November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code NTE, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260