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
K873809Substantially Equivalent

Excalibur Electrosurgical Unit 60-5200-001

Zimmer Aspen Labs, Englewood CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K873809 is the FDA 510(k) clearance record for EXCALIBUR ELECTROSURGICAL UNIT 60-5200-001, a class II device, cleared for Zimmer Aspen Labs on under FDA product code BWA (Unit, Electrosurgical And Coagulation, With Accessories). FDA records list one 510(k) clearance for Zimmer Aspen Labs. As of , FDA records show no recalls naming K873809.

Clearance record

Decision date
Received
(63 days to decision)
Product code
BWA Unit, Electrosurgical And Coagulation, With Accessories
Regulation
21 CFR 878.4400
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Zimmer Aspen Labs P.O. Box 3936, Englewood CO
Third party review
No

Clearances, product code BWA

Trailing 12 months

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

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