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MotoBAND CP Locking Drill Guide

FDA UDI

Class I (US FDA UDI)

by Crossroads Extremity Systems Llc

Identity

Trade Name
MotoBAND CP Locking Drill Guide FDA UDI
Generic Name
Orthopaedic bone wire FDA UDI
Device Name
The MotoBAND™ CP Implant System is a bone plating system 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. It consist of plates and screws. FDA UDI
Model / Reference
130500 FDA UDI
Description
The MotoBAND™ CP Implant System is a bone plating system 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. It consist of plates and screws. FDA UDI

Identifiers

Catalog Number
130500 FDA UDI
Primary DI / UDI-DI
00815432028429 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic bone wire FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical drill guide, reusableOrthopaedic bone wire

MotoBAND CP Locking Drill Guide by Crossroads Extremity Systems Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone wire.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 165eeb2b-bd91-40e9-8885-e21478e32e6d 34 fields · synced May 30, 2026