MotoBAND CP DynaFORCE™ - The MotoBAND® CP Implant System is indicated for - CROSSROADS EXTREMITY SYSTEMS

Duns Number:058864308

Device Description: The MotoBAND® CP Implant System is indicated for stabilization and fixation of fresh fract The MotoBAND® CP Implant System is indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. When used for these indications, the MotoBAND® CP Implant System with the exception of the 2-hole plate may be used with the MotoCLIP®/HiMAX® Implant System.

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More Product Details

Catalog Number

280293

Brand Name

MotoBAND CP DynaFORCE™

Version/Model Number

DynaBunion Reducer Knob

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

-

Product Code Details

Product Code

LXH

Product Code Name

Orthopedic Manual Surgical Instrument

Device Record Status

Public Device Record Key

ac64bc92-c7b7-451b-98cd-b54822bf881f

Public Version Date

July 23, 2020

Public Version Number

2

DI Record Publish Date

May 15, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"CROSSROADS EXTREMITY SYSTEMS" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 59
2 A medical device with a moderate to high risk that requires special controls. 713