Cleared Traditional

K150796 - Dental Bone Cutting Instruments

K150796 is the FDA 510(k) clearance for Dental Bone Cutting Instruments by Synthes USA Products, LLC. It is a Class 2 Dental device (product code DZJ) cleared through the Traditional 510(k) pathway after a 89-day FDA review.

K150796 · Synthes USA Products, LLC · Dental device
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Jun 2015
Decision
89d
Days
Class 2
Risk

K150796 is an FDA 510(k) clearance for the Dental Bone Cutting Instruments. Classified as Driver, Wire, And Bone Drill, Manual (product code DZJ), Class II - Special Controls.

Submitted by Synthes USA Products, LLC (West Chester, US). The FDA issued a Cleared decision on June 23, 2015 after a review of 89 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.4120 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Synthes USA Products, LLC devices

Submission Details

510(k) Number K150796 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 26, 2015
Decision Date June 23, 2015
Days to Decision 89 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
38d faster than avg
Panel avg: 127d · This submission: 89d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DZJ Driver, Wire, And Bone Drill, Manual
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.4120
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 - DZJ Driver, Wire, And Bone Drill, Manual

All 21
Devices cleared under the same product code (DZJ) and FDA review panel - the closest regulatory comparables to K150796.
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K040369 · Stryker Instruments · Apr 2004
SURGICAL CUTTING BURS
K943540 · Stryker Corp. · Nov 1994