Cleared Traditional

K073161 - REPLUS DENTAL IMPLANTS (HA)

K073161 is an FDA 510(k) clearance for REPLUS DENTAL IMPLANTS (HA), manufactured by Implant Direct, LLC. The device is a Class 2 Dental device with product code DZE cleared through the Traditional 510(k) pathway after a 119-day FDA review.

K073161 · Implant Direct, LLC · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 2008
Decision
119d
Days
Class 2
Risk

K073161 is an FDA 510(k) clearance for the REPLUS DENTAL IMPLANTS (HA). Classified as Implant, Endosseous, Root-form (product code DZE), Class II - Special Controls.

Submitted by Implant Direct, LLC (Calabasas, US). The FDA issued a Cleared decision on March 7, 2008 after a review of 119 days - within the typical 510(k) review window.

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 Implant Direct, LLC devices

FDA 510(k) Submission Details - K073161

510(k) Number K073161 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 09, 2007
Decision Date March 07, 2008
Days to Decision 119 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
8d faster than avg
Panel avg: 127d · This submission: 119d
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 934
Devices cleared under the same product code (DZE) and FDA review panel - the closest regulatory comparables to K073161.
BLUE SKY BIO DENTAL IMPLANT SYSTEM
K073713 · Blue Sky Bio, LLC · Mar 2008
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JNE IMPLANT SYSTEM
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US/SS/GS SYSTEM
K073247 · Osstem Implant Co., Ltd. · Mar 2008
HU II / HS II FIXTURE SYSTEM
K080387 · Osstem Implant Co., Ltd. · Mar 2008
ANKYLOS DENTAL IMPLANT SYSTEM/CLAIMS
K073067 · Dentsply International, Inc. · Feb 2008