Cleared Traditional

K092743 - THE LEIBINGER ADVANCE INTERNAL MIDFACE ...

K092743 is an FDA 510(k) clearance for THE LEIBINGER ADVANCE INTERNAL MIDFACE ..., manufactured by Stryker Craniomaxillofacial. The device is a Class 2 Dental device with product code JEY cleared through the Traditional 510(k) pathway after a 129-day FDA review.

K092743 · Stryker Craniomaxillofacial · Dental device
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Jan 2010
Decision
129d
Days
Class 2
Risk

K092743 is an FDA 510(k) clearance for the THE LEIBINGER ADVANCE INTERNAL MIDFACE DISTRACTION SYSTEM. Classified as Plate, Bone (product code JEY), Class II - Special Controls.

Submitted by Stryker Craniomaxillofacial (Kalamazoo, US). The FDA issued a Cleared decision on January 15, 2010 after a review of 129 days - within the typical 510(k) review window.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.4760 - the FDA dental device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Dental review framework, consistent with the majority of Class II 510(k) submissions.

View all Stryker Craniomaxillofacial devices

FDA 510(k) Submission Details - K092743

510(k) Number K092743 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 08, 2009
Decision Date January 15, 2010
Days to Decision 129 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
2d slower than avg
Panel avg: 127d · This submission: 129d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JEY Device Classification - Class 2, Special Controls

Product Code JEY Plate, Bone
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.4760
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Dental devices follow this clearance model.

Regulatory Peers - JEY Plate, Bone

All 198
Devices cleared under the same product code (JEY) and FDA review panel - the closest regulatory comparables to K092743.
LEFORTE NEURO SYSTEM BONE PLATE
K103778 · Jeil Medical Corporation · Jan 2011
SYNTHES DENTOALVEOLAR BONE FIXATION SYSTEM
K102656 · Synthes (Usa) · Dec 2010
SUSTAIN SPACE MAINTENANCE SYSTEM
K100779 · Medtronic Sofamor Danek USA, Inc. · Dec 2010
SYNTHES MATRIXMANDIBLE SUBCONDYLAR PLATES
K091233 · Synthes (Usa) · Dec 2009
LEFORTE SYSTEM BONE PLATE
K091679 · Jeil Medical Corporation · Oct 2009
SYNTHES MATRIXMANDIBLE PREFORMED RECONSTRUCTION PLATES
K091144 · Synthes (Usa) · Aug 2009