510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K982269Substantially Equivalent

Clear Hub Spinal Needle 14Ga, 16Ga, 17Ga, 18Ga, 20Ga, 21Ga, 22Ga, 25Ga, 26Ga and 27Ga

Medtronic, Inc., Mcgraw Park IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K982269 is the FDA 510(k) clearance record for CLEAR HUB SPINAL NEEDLE 14GA, 16GA, 17GA, 18GA, 20GA, 21GA, 22GA, 25GA, 26GA AND 27GA, a class II device, cleared for Allegiance Healthcare Corp. on under FDA product code MIA (Needle, Spinal, Short Term). FDA records list 1,525 510(k) clearances for Medtronic, Inc., from to . As of , FDA records show no recalls naming K982269.

Clearance record

Decision date
Received
(24 days to decision)
Product code
MIA Needle, Spinal, Short Term
Regulation
21 CFR 868.5150
Device class
Class II
Review panel
Anesthesiology
Applicant
Allegiance Healthcare Corp. 1500 Waukegan Rd.- K, Mcgraw Park IL
510(k) summary
Summary
Third party review
No

Clearances, product code MIA

Trailing 12 months

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

FDA records show no clearances under product code MIA in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MIA, 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