Cleared Traditional

K062851 - OSTEOMED PEDIATRIC INTRAORAL MANDIBULAR DISTRACTION SYSTEM, EXTENDED

K062851 is an FDA 510(k) clearance for OSTEOMED PEDIATRIC INTRAORAL MANDIBULAR..., manufactured by Osteomed LP. The device is a Class 2 Dental device with product code MQN cleared through the Traditional 510(k) pathway after a 53-day FDA review.

K062851 · Osteomed LP · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Nov 2006
Decision
53d
Days
Class 2
Risk

K062851 is an FDA 510(k) clearance for the OSTEOMED PEDIATRIC INTRAORAL MANDIBULAR DISTRACTION SYSTEM, EXTENDED. Classified as External Mandibular Fixator And/or Distractor (product code MQN), Class II - Special Controls.

Submitted by Osteomed LP (Addison, US). The FDA issued a Cleared decision on November 17, 2006 after a review of 53 days - a notably fast clearance cycle.

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: 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 Osteomed LP devices

FDA 510(k) Submission Details - K062851

510(k) Number K062851 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 25, 2006
Decision Date November 17, 2006
Days to Decision 53 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
74d faster than avg
Panel avg: 127d · This submission: 53d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MQN Device Classification - Class 2, Special Controls

Product Code MQN External Mandibular Fixator And/or Distractor
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 - MQN External Mandibular Fixator And/or Distractor

All 56
Devices cleared under the same product code (MQN) and FDA review panel - the closest regulatory comparables to K062851.
STRYKER EXTERNAL FIXATION SYSTEM
K071628 · Stryker Cmf · Aug 2007
CRANIOTECH BONE TRANSPORT RECONSTRUCTION PLATE
K062572 · Custom Scientific · May 2007
OSTEOMED EXTERNAL MANDIBULAR DISTRACTION SYSTEM
K063792 · Osteomed LP · Mar 2007
SYNTHES STERILE MANDIBLE EXTERNAL FIXATION KIT
K062299 · Synthes (Usa) · Aug 2006
SYNTHES (USA) CRANIOMAXILLOFACIAL DISTRACTION SYSTEM
K060138 · Synthes (Usa) · Jun 2006
MODUS MODULAR DISTRACTION OSTEOGENESIS SYSTEM
K051946 · Medartis, Inc. · Aug 2005