510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K160296Substantially Equivalent

SPROTTE SPECIAL NRFit

Pajunk GmbH Medizintechnologie, Geisingen, DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K160296 is the FDA 510(k) clearance record for SPROTTE SPECIAL NRFit, a class II device, cleared for PAJUNK GmbH Medizintechnologie on under FDA product code BSP (Needle, Conduction, Anesthetic (W/Wo Introducer)). FDA records list 63 510(k) clearances for PAJUNK GmbH Medizintechnologie, from to . As of , FDA records show no recalls naming K160296.

Clearance record

Decision date
Received
(267 days to decision)
Product code
BSP Needle, Conduction, Anesthetic (W/Wo Introducer)
Regulation
21 CFR 868.5150
Device class
Class II
Review panel
Anesthesiology
Applicant
PAJUNK GmbH Medizintechnologie Karl-Hall St. 1, Geisingen, DE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code BSP

Trailing 12 months

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

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