Cleared Special

K983786 - STERNGOLD IMPLAMED WIDE PLATFORM DENTAL IMPLANTS AND RELATED PROSTHETICS AND INSTTUMENTATION

K983786 is an FDA 510(k) clearance for STERNGOLD IMPLAMED WIDE PLATFORM DENTAL..., manufactured by Sterngold/Implamed. The device is a Class 2 Dental device with product code DZE cleared through the Special 510(k) pathway after a 17-day FDA review.

K983786 · Sterngold/Implamed · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Nov 1998
Decision
17d
Days
Class 2
Risk

K983786 is an FDA 510(k) clearance for the STERNGOLD IMPLAMED WIDE PLATFORM DENTAL IMPLANTS AND RELATED PROSTHETICS AND .... Classified as Implant, Endosseous, Root-form (product code DZE), Class II - Special Controls.

Submitted by Sterngold/Implamed (Attleboro, US). The FDA issued a Cleared decision on November 13, 1998 after a review of 17 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. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Sterngold/Implamed devices

FDA 510(k) Submission Details - K983786

510(k) Number K983786 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 27, 1998
Decision Date November 13, 1998
Days to Decision 17 days
Submission Type Special
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
110d faster than avg
Panel avg: 127d · This submission: 17d
Pathway characteristics
Modification to existing cleared device.

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 1318
Devices cleared under the same product code (DZE) and FDA review panel - the closest regulatory comparables to K983786.
IMCOR 4.00 & 5.00MM SELF-TAPPING LOCKTITE IMPLANTS, IMCOR 4.00 & 5.00MM SELF-TAPPING HA COASTED LOCKTITE IMPLANTS, AND I
K983563 · Imcor · Jan 1999
OSSEOTITE DENTAL IMPLANTS
K983347 · Implant Innovations, Inc. · Jan 1999
ASTRA TECH IMPLANT DENTAL SYSTEM
K974738 · Astra Tech, Inc. · Nov 1998
FRIALIT-2 AUROBASE MODEL NUMBERS 45-2446, 45-2456, 45-2466, 45-2476
K982576 · Friatec AG · Oct 1998
IMCOR DENTAL IMPLANT SYSTEM ACCESSORIES
K982492 · Imcor · Oct 1998
SPLINE DENTAL IMPLANT SYSTEM-TEMPORARY ABUTMENT
K982305 · Sulzer Calcitek, Inc. · Sep 1998