510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K902259Substantially Equivalent for Some Indications

Axiom Total Knee System, Tibial Component

Orthomet, Inc., Minneapolis MN / Traditional, Substantially Equivalent for Some Indications
FDA source (opens on fda.gov)

K902259 is the FDA 510(k) clearance record for AXIOM TOTAL KNEE SYSTEM, TIBIAL COMPONENT, a class I device, cleared for Orthomet, Inc. on under FDA product code JWX (Kit, Screening, Staphylococcus Aureus). FDA records list 60 510(k) clearances for Orthomet, Inc., from to . As of , FDA records show no recalls naming K902259.

Clearance record

Decision date
Received
(28 days to decision)
Product code
JWX Kit, Screening, Staphylococcus Aureus
Regulation
21 CFR 866.2660
Device class
Class I
Review panel
Microbiology
Applicant
Orthomet, Inc. 6301 Cecilia Cir., Minneapolis MN
Third party review
No

Clearances, product code JWX

Trailing 12 months

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

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