510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K172800Substantially Equivalent

Portex® Lancet Point Spinal Needles with NRFit™ connectors, Portex® Pencil Point Spinal Needles with NRFit™ connectors

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

K172800 is the FDA 510(k) clearance record for Portex® Lancet Point Spinal Needles with NRFit™ connectors, Portex® Pencil Point Spinal Needles with NRFit™ connectors, a class II device, cleared for Smiths Medical Asd, Inc. on under FDA product code MIA (Needle, Spinal, Short Term). FDA records list 1,478 510(k) clearances for Abbott Medical, from to . As of , FDA records show no recalls naming K172800.

Clearance record

Decision date
Received
(269 days to decision)
Product code
MIA Needle, Spinal, Short Term
Regulation
21 CFR 868.5150
Device class
Class II
Review panel
Anesthesiology
Applicant
Smiths Medical Asd, Inc. 6000 Nathan Ln. N, Plymouth MN
510(k) summary
Summary PDF
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