MotoCLIP/HiMAX Step Staple 7200-ST12KT

GUDID 00815432026494

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

CROSSROADS EXTREMITY SYSTEMS

Orthopaedic bone staple, non-adjustable, sterile
Primary Device ID00815432026494
NIH Device Record Keyd42e9f2a-1f7c-4eab-8192-4a0be365017d
Commercial Distribution StatusIn Commercial Distribution
Brand NameMotoCLIP/HiMAX Step Staple
Version Model NumberImplant Kit, 18mm x 22mm x 24mm, 12mm Offset
Catalog Number7200-ST12KT
Company DUNS058864308
Company NameCROSSROADS EXTREMITY SYSTEMS
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone901-221-8406
Emailinfo@crextremity.com
Phone901-221-8406
Emailinfo@crextremity.com
Phone901-221-8406
Emailinfo@crextremity.com
Phone901-221-8406
Emailinfo@crextremity.com
Phone901-221-8406
Emailinfo@crextremity.com
Phone901-221-8406
Emailinfo@crextremity.com
Phone901-221-8406
Emailinfo@crextremity.com
Phone901-221-8406
Emailinfo@crextremity.com
Phone901-221-8406
Emailinfo@crextremity.com
Phone901-221-8406
Emailinfo@crextremity.com
Phone901-221-8406
Emailinfo@crextremity.com
Phone901-221-8406
Emailinfo@crextremity.com
Phone901-221-8406
Emailinfo@crextremity.com
Phone901-221-8406
Emailinfo@crextremity.com
Phone901-221-8406
Emailinfo@crextremity.com
Phone901-221-8406
Emailinfo@crextremity.com
Phone901-221-8406
Emailinfo@crextremity.com
Phone901-221-8406
Emailinfo@crextremity.com
Phone901-221-8406
Emailinfo@crextremity.com

Device Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
GS100815432026494 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JDRStaple, Fixation, Bone

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-12-13
Device Publish Date2018-11-12

On-Brand Devices [MotoCLIP/HiMAX Step Staple]

00815432026517MotoCLIP/HiMAX Step Staple Implant System is a Nitinol Superelastic bone staple for use in surge
00815432026494MotoCLIP/HiMAX Step Staple Implant System is a Nitinol Superelastic bone staple for use in surge
00815432026487MotoCLIP/HiMAX Step Staple Implant System is a Nitinol Superelastic bone staple for use in surge
00815432026470MotoCLIP/HiMAX Step Staple Implant System is a Nitinol Superelastic bone staple for use in surge
00815432026463MotoCLIP/HiMAX Step Staple Implant System is a Nitinol Superelastic bone staple for use in surge
00815432026456MotoCLIP/HiMAX Step Staple Implant System is a Nitinol Superelastic bone staple for use in surge
00815432026432MotoCLIP/HiMAX Step Staple Implant System is a Nitinol Superelastic bone staple for use in surge
00815432026425MotoCLIP/HiMAX Step Staple Implant System is a Nitinol Superelastic bone staple for use in surge
00815432026418MotoCLIP/HiMAX Step Staple Implant System is a Nitinol Superelastic bone staple for use in surge
00815432026401MotoCLIP/HiMAX Step Staple Implant System is a Nitinol Superelastic bone staple for use in surge
00815432026395MotoCLIP/HiMAX Step Staple Implant System is a Nitinol Superelastic bone staple for use in surge

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