HiMAX C 7118-1414-C

GUDID 00815432026265

MotoCLIP/HiMAX Impant 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 ID00815432026265
NIH Device Record Key2547dc79-fc2d-481c-860d-78ad7fba8326
Commercial Distribution StatusIn Commercial Distribution
Brand NameHiMAX C
Version Model Number7118-1414-C
Catalog Number7118-1414-C
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

Device Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
GS100815432026265 [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 Date2019-03-11
Device Publish Date2019-02-20

On-Brand Devices [HiMAX C]

00815432026289MotoCLIP/HiMAX Impant System is a Nitinol Superelastic bone staple for use in surgery of the han
00815432026272MotoCLIP/HiMAX Impant System is a Nitinol Superelastic bone staple for use in surgery of the han
00815432026173MotoCLIP/HiMAX Implant System is a Nitinol Superelastic bone staple for use in surgery of the ha
00815432026166MotoCLIP/HiMAX Implant System is a Nitinol Superelastic bone staple for use in surgery of the ha
00815432026265MotoCLIP/HiMAX Impant System is a Nitinol Superelastic bone staple for use in surgery of the han
00815432026159MotoCLIP/HiMAX Implant System is a Nitinol Superelastic bone staple for use in surgery of the ha
00815432028894MotoCLIP/HiMAX Impant System is a Nitinol Superelastic bone staple for use in surgery of the han
00815432028900MotoCLIP/HiMAX Implant System is a Nitinol Superelastic bone staple for use in surgery of the ha
00815432026340MotoCLIP/HiMAX Implant System is a Nitinol Superelastic bone staple for use in surgery of the ha
00815432026203MotoCLIP/HiMAX Implant System is a Nitinol Superelastic bone staple for use in surgery of the ha
00815432026197MotoCLIP/HiMAX Implant System is a Nitinol Superelastic bone staple for use in surgery of the ha
00815432026180MotoCLIP/HiMAX Implant System is a Nitinol Superelastic bone staple for use in surgery of the ha
00815432026142MotoCLIP/HiMAX Implant System is a Nitinol Superelastic bone staple for use in surgery of the ha
00815432026135MotoCLIP/HiMAX Implant System is a Nitinol Superelastic bone staple for use in surgery of the ha
00815432026258MotoCLIP/HiMAX Implant System is a Nitinol Superelastic bone staple for use in surgery of the ha
00815432026241MotoCLIP/HiMAX Implant System is a Nitinol Superelastic bone staple for use in surgery of the ha
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