Integra® MOVEMENT® Great Toe System - The Integra Movement Great Toe System metatarsal - Ascension Orthopedics, Inc.

Duns Number:942377524

Device Description: The Integra Movement Great Toe System metatarsal component is designed for resurfacing the The Integra Movement Great Toe System metatarsal component is designed for resurfacing the 1st metatarsal head. The component is an anatomically designed, monolithic device.The device is made from cobalt chromium alloy with a commercially pure titanium plasma spray. The metatarsal is intended as hemi-arthroplasty at the surface and is a press-fit.

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More Product Details

Catalog Number

MGT89020MT

Brand Name

Integra® MOVEMENT® Great Toe System

Version/Model Number

MGT89020MT

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K092047

Product Code Details

Product Code

KWD

Product Code Name

PROSTHESIS, TOE, HEMI-, PHALANGEAL

Device Record Status

Public Device Record Key

9626e496-ccf0-4c30-ad9f-c83434a3d475

Public Version Date

April 21, 2021

Public Version Number

4

DI Record Publish Date

October 09, 2017

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ASCENSION ORTHOPEDICS, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1909
2 A medical device with a moderate to high risk that requires special controls. 1404
3 A medical device with high risk that requires premarket approval 12
U Unclassified 15