Micro 2 System

FDA 510(k) K900785 · Inodent

Substantially Equivalent

510(k) numberK900785

Submission

Device name
Micro 2 System
Applicant
Inodent
Washington, DC, US
Received
February 20, 1990
Decision date
April 16, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
EGG – Attachment, Precision, All
Device class
Class I (low risk)
Regulation
21 CFR 872.3165
Specialty
Dental

Other 510(k)s with product code EGG

510(k)DeviceApplicantDecision
K990979Steco-TitanmagneticsEGG · Traditional Steco-System-Technik GmbH & Cokg09/03/1999SE
K950259Coupling Device for Dental ProsthesisEGG · Traditional Dr. Joseph E. Grasso, D.D.S.12/06/1996SE
K925700Zest Anchor Advanced GenerationEGG · Traditional Zest Anchors, Inc.04/07/1994SE
K915299Cogan Corp Kits of Dental Hand InstrumentsEGG · Traditional Cogan Corp.01/31/1992SE
K912435Dental Connector Precision AttachmentEGG · Traditional Metalor Dental USA Corp.08/28/1991SE
K912567Conicast, Intracast, OmecastEGG · Traditional Metalor Dental USA Corp.07/02/1991SE
K901928Interpore Imz(Castable)Tub/Scret Ret Rigid AttachEGG · Traditional Interpore Intl.07/26/1990SE
K896337Dental Bridge Anchoring PinsEGG · Traditional Gayso Bridge-Tech, Inc.01/31/1990SE
K895986Precision Dental AttachmentsEGG · Traditional Implant Support Systems, Inc.10/18/1989SE
K891119T.R.S.: Tooth Replacement SystemEGG · Traditional Health Technology of America, Inc.04/17/1989SE

Questions and answers

When was Micro 2 System cleared by the FDA?

Micro 2 System (K900785) received a 510(k) decision of Substantially Equivalent on April 16, 1990, 55 days after the submission was received.

What is the product code of K900785?

The FDA product code is EGG – Attachment, Precision, All, a Class I (low risk) device regulated under 21 CFR 872.3165.