Cleared Traditional

K051798 - OSTEOMED ORTHODONTIC ANCHOR PLATING SYSTEM

K051798 is an FDA 510(k) clearance for OSTEOMED ORTHODONTIC ANCHOR PLATING SYSTEM, manufactured by Osteomed LP. The device is a Class 2 Dental device with product code DZE cleared through the Traditional 510(k) pathway after a 276-day FDA review.

K051798 · Osteomed LP · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 2006
Decision
276d
Days
Class 2
Risk

K051798 is an FDA 510(k) clearance for the OSTEOMED ORTHODONTIC ANCHOR PLATING SYSTEM. Classified as Implant, Endosseous, Root-form (product code DZE), Class II - Special Controls.

Submitted by Osteomed LP (Addison, US). The FDA issued a Cleared decision on April 7, 2006 after a review of 276 days - an extended review cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3640 - 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 Osteomed LP devices

FDA 510(k) Submission Details - K051798

510(k) Number K051798 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 05, 2005
Decision Date April 07, 2006
Days to Decision 276 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
149d slower than avg
Panel avg: 127d · This submission: 276d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DZE Device Classification - Class 2, Special Controls

Product Code DZE Implant, Endosseous, Root-form
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3640
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 - DZE Implant, Endosseous, Root-form

All 1268
Devices cleared under the same product code (DZE) and FDA review panel - the closest regulatory comparables to K051798.
SIMPLER HA THREADED, ST 5002-8, SIT 5002-8, ST 5011-ST5014, ST 5021-24
K060376 · Simpler Implant, Inc. · Apr 2006
RESCUE IMPLANT SYSTEM
K053353 · Megagen Co., Ltd. · Apr 2006
INTERMEZZO PLUS FIXTURE
K053354 · Megagen Co., Ltd. · Apr 2006
ENDOSSEOUS DENTAL IMPLANT SYSTEM
K053478 · Northern Implants, LLC · Apr 2006
FIXATURE MICROTHREAD OSSEOSPEED, A COMPONENT OF THE ASTRA TECH IMPLANT SYSTEM
K053384 · Astra Tech, Inc. · Mar 2006
A.B. DENTAL DEVICES
K051719 · A.B. Dental Devices , Ltd. · Mar 2006