Cleared Traditional

K102656 - SYNTHES DENTOALVEOLAR BONE FIXATION SYSTEM

K102656 is the FDA 510(k) clearance for SYNTHES DENTOALVEOLAR BONE FIXATION SYSTEM by Synthes (Usa). It is a Class 2 Dental device (product code JEY) cleared through the Traditional 510(k) pathway after a 96-day FDA review.

K102656 · Synthes (Usa) · Dental device
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Dec 2010
Decision
96d
Days
Class 2
Risk

K102656 is an FDA 510(k) clearance for the SYNTHES DENTOALVEOLAR BONE FIXATION SYSTEM. Classified as Plate, Bone (product code JEY), Class II - Special Controls.

Submitted by Synthes (Usa) (West Chester, US). The FDA issued a Cleared decision on December 20, 2010 after a review of 96 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 Synthes (Usa) devices

Submission Details

510(k) Number K102656 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 15, 2010
Decision Date December 20, 2010
Days to Decision 96 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
31d faster than avg
Panel avg: 127d · This submission: 96d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 156
Devices cleared under the same product code (JEY) and FDA review panel - the closest regulatory comparables to K102656.
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LEFORTE NEURO SYSTEM BONE PLATE
K103778 · Jeil Medical Corporation · Jan 2011
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