Cleared Traditional

K052061 - MODUS IMF SCREWS 2.0

K052061 is an FDA 510(k) clearance for MODUS IMF SCREWS 2.0, manufactured by Medartis, Inc.. The device is a Class 2 Dental device with product code DZE cleared through the Traditional 510(k) pathway after a 84-day FDA review.

K052061 · Medartis, Inc. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 2005
Decision
84d
Days
Class 2
Risk

K052061 is an FDA 510(k) clearance for the MODUS IMF SCREWS 2.0. Classified as Implant, Endosseous, Root-form (product code DZE), Class II - Special Controls.

Submitted by Medartis, Inc. (San Diego, US). The FDA issued a Cleared decision on October 21, 2005 after a review of 84 days - a notably fast clearance 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: 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 Medartis, Inc. devices

FDA 510(k) Submission Details - K052061

510(k) Number K052061 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 29, 2005
Decision Date October 21, 2005
Days to Decision 84 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
43d faster than avg
Panel avg: 127d · This submission: 84d
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 759
Devices cleared under the same product code (DZE) and FDA review panel - the closest regulatory comparables to K052061.
SLACTIVE IMPLANTS
K053088 · Institut Straumann AG · Feb 2006
ZIMMER DENTAL ONE-PIECE IMPLANT
K052997 · Zimmer Dental, Inc. · Jan 2006
BIOHORIZONS SINGLE-STAGE IMPLANT
K053152 · BioHorizons Implant Systems, Inc. · Dec 2005
MAXIMUS 3.0 AND OS IMPLANTS
K052419 · BioHorizons Implant Systems, Inc. · Sep 2005
3I OSSEOTITE DENTAL IMPLANTS
K051461 · Implant Innovations, Inc. · Sep 2005
PRIMACONNEX INTERNAL CONNECTION IMPLANT SYSTEM, PRIMACONNEX INTERNAL CONNECTION PROSTHETICS
K051614 · Lifecore Biomedical, Inc. · Sep 2005