510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K031959Substantially Equivalent

Stryker Plating System Periarticular Plates

Howmedica Osteonics Corp, Allendale NJ / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K031959 is the FDA 510(k) clearance record for STRYKER PLATING SYSTEM PERIARTICULAR PLATES, a class II device, cleared for Howmedica Osteonics Corp. on under FDA product code LXT (Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite). FDA records list 377 510(k) clearances for Howmedica Osteonics Corp., from to . As of , FDA records show no recalls naming K031959.

Clearance record

Decision date
Received
(30 days to decision)
Product code
LXT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite
Regulation
21 CFR 888.3030
Device class
Class II
Review panel
Orthopedic
Applicant
Howmedica Osteonics Corp. 59 Rte. 17 S., Allendale NJ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LXT

Trailing 12 months

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

FDA records show no clearances under product code LXT in the twelve months to November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LXT, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260