Cleared Traditional

K871834 - DRILL, HAND, BONE, SMEDBERG (FDA 510(k) Clearance)

Class II Dental device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 1987
Decision
80d
Days
Class 2
Risk

K871834 is an FDA 510(k) clearance for the DRILL, HAND, BONE, SMEDBERG. Classified as Driver, Wire, And Bone Drill, Manual (product code DZJ), Class II - Special Controls.

Submitted by Military Engineering, Inc. (Plymouth, US). The FDA issued a Cleared decision on July 31, 1987 after a review of 80 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 Military Engineering, Inc. devices

Submission Details

510(k) Number K871834 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 12, 1987
Decision Date July 31, 1987
Days to Decision 80 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
47d faster than avg
Panel avg: 127d · This submission: 80d
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 30
Devices cleared under the same product code (DZJ) and FDA review panel - the closest regulatory comparables to K871834.
Materialise Personalized Guides and Models for Craniomaxillofacial Surgery
K243637 · Materialise NV · Feb 2025
TECHFIT DISRP® System
K242263 · Techfit Digital Surgery, Inc. · Dec 2024
tmCMF Solution
K231520 · Techmah Cmf · Oct 2023
TECHFIT DISRP® System
K230276 · Techfit Digital Surgery · Jun 2023
MedCAD AccuPlan System
K223024 · Medcad · Mar 2023
EmbedMed
K220366 · 3D Lifeprints UK , Ltd. · Sep 2022