510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K072371Substantially Equivalent

Odyssey Workstation

Stereotaxis Inc, St. Louis MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K072371 is the FDA 510(k) clearance record for ODYSSEY WORKSTATION, a class II device, cleared for Stereotaxis, Inc. on under FDA product code DXX (System, Catheter Control, Steerable). FDA records list 28 510(k) clearances for Stereotaxis, Inc., from to . As of , FDA records show no recalls naming K072371.

Clearance record

Decision date
Received
(83 days to decision)
Product code
DXX System, Catheter Control, Steerable
Regulation
21 CFR 870.1290
Device class
Class II
Review panel
Cardiovascular
Applicant
Stereotaxis, Inc. 4320 Forest Park Ave., Suite 100, St. Louis MO
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DXX

Trailing 12 months
2 clearances under product code DXX in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DXX, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20261
September 20260
October 20260