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MotoCLIP/HiMAX Step Staple

FDA UDI

Class II (US FDA UDI)

by Crossroads Extremity Systems Llc

Identity

Trade Name
MotoCLIP/HiMAX Step Staple FDA UDI
Generic Name
Orthopaedic bone staple, non-adjustable FDA UDI
Device Name
MotoCLIP/HiMAX Step Staple Implant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis FDA UDI
Model / Reference
Single Pack, 18mm x 22mm x 24mm, 8mm Offset FDA UDI
Description
MotoCLIP/HiMAX Step Staple Implant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis FDA UDI

Identifiers

Catalog Number
7200-ST08 FDA UDI
Primary DI / UDI-DI
00815432026418 FDA UDI
510(k) Number
K181866 FDA UDI
FDA Product Code
JDR FDA UDI
GMDN Term
Orthopaedic bone staple, non-adjustable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic bone staple, non-adjustable

MotoCLIP/HiMAX Step Staple by Crossroads Extremity Systems Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone staple, non-adjustable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f45f618a-7298-4995-a927-60a4735eff05 37 fields · synced May 30, 2026