510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K811223Substantially Equivalent

Vasovasostomy Stabilizer Platform Dev

Zimmer GmbH, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K811223 is the FDA 510(k) clearance record for VASOVASOSTOMY STABILIZER PLATFORM DEV, a class I device, cleared for Biomet, Inc. on under FDA product code KOA (Surgical Instruments, G-U, Manual (And Accessories)). FDA records list 872 510(k) clearances for ZIMMER GMBH, from to . As of , FDA records show no recalls naming K811223.

Clearance record

Decision date
Received
(17 days to decision)
Product code
KOA Surgical Instruments, G-U, Manual (And Accessories)
Regulation
21 CFR 876.4730
Device class
Class I
Review panel
Gastroenterology, Urology
Applicant
Biomet, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KOA

Trailing 12 months

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

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