510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K013120Substantially Equivalent

Percutaneous Introducer Set, Model 042294 and Kit Model 3550-18

Greatbatch Medical, Minneapolis MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K013120 is the FDA 510(k) clearance record for PERCUTANEOUS INTRODUCER SET, MODEL 042294 AND KIT MODEL 3550-18, a class II device, cleared for Medamicus, Inc. on under FDA product code GZB (Stimulator, Spinal-Cord, Implanted (Pain Relief)). FDA records list 25 510(k) clearances for Greatbatch Medical, from to . As of , FDA records show no recalls naming K013120.

Clearance record

Decision date
Received
(128 days to decision)
Product code
GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
Regulation
21 CFR 882.5880
Device class
Class II
Review panel
Neurology
Applicant
Medamicus, Inc. 15301 Hwy. 55 W., Minneapolis MN
510(k) summary
Summary
Third party review
No

Clearances, product code GZB

Trailing 12 months

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

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