510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K072155Substantially Equivalent

Pioneer Catheter

Medtronic, Inc., Santa Rosa CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K072155 is the FDA 510(k) clearance record for PIONEER CATHETER, a class II device, cleared for Medtronic, Inc. on under FDA product code PDU (Catheter For Crossing Total Occlusions). FDA's definition for product code PDU reads: "To facilitate the intraluminal placement of conventional guidewires beyond stenotic lesions (including subchronic and chronic total occlusions) in the peripheral vasculature prior to further percutaneous intervention, such as angioplasty...". FDA records list 1,525 510(k) clearances for Medtronic, Inc., from to . As of , FDA records show no recalls naming K072155.

Clearance record

Decision date
Received
(63 days to decision)
Product code
PDU Catheter For Crossing Total Occlusions
Regulation
21 CFR 870.1250
Device class
Class II
Review panel
Cardiovascular
Applicant
Medtronic, Inc. 3576 Unocal Pl., Santa Rosa CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code PDU

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