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
K894240Substantially Equivalent

Neos 02

Biotronik Cardiac Pacemakers, Lake Oswego CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K894240 is the FDA 510(k) clearance record for NEOS 02, a class III device, cleared for Biotronik Cardiac Pacemakers on under FDA product code DXY (Implantable Pacemaker Pulse-Generator). FDA records list 3 510(k) clearances for Biotronik Cardiac Pacemakers, from to . As of , FDA records show no recalls naming K894240.

Clearance record

Decision date
Received
(128 days to decision)
Product code
DXY Implantable Pacemaker Pulse-Generator
Regulation
21 CFR 870.3610
Device class
Class III
Review panel
Cardiovascular
Applicant
Biotronik Cardiac Pacemakers P.O. Box 1988, Lake Oswego CA
Third party review
No

Clearances, product code DXY

Trailing 12 months

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

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