510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K092743Substantially Equivalent

The Leibinger Advance Internal Midface Distraction System

Stryker Craniomaxillofacial, Kalamazoo MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K092743 is the FDA 510(k) clearance record for THE LEIBINGER ADVANCE INTERNAL MIDFACE DISTRACTION SYSTEM, a class II device, cleared for Stryker Craniomaxillofacial on under FDA product code JEY (Plate, Bone). FDA records list 3 510(k) clearances for Stryker Craniomaxillofacial, from to . As of , FDA records show no recalls naming K092743.

Clearance record

Decision date
Received
(129 days to decision)
Product code
JEY Plate, Bone
Regulation
21 CFR 872.4760
Device class
Class II
Review panel
Dental
Applicant
Stryker Craniomaxillofacial 750 Trade Centre Way, Kalamazoo MI
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JEY

Trailing 12 months
5 clearances under product code JEY 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 JEY, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20261
August 20261
September 20260
October 20260