0840040350

GUDID 04546540130372

2.5 inch (63.5mm) Titanium Nitrided Blade

STRYKER CORPORATION

Cast cutter blade
Primary Device ID04546540130372
NIH Device Record Key3c6b0f89-8ccd-4a47-8fdb-6ab1a32533cb
Commercial Distribution StatusIn Commercial Distribution
Version Model Number0840040350
Catalog Number0840040350
Company DUNS196548481
Company NameSTRYKER CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS104546540130372 [Primary]

FDA Product Code

LGHINSTRUMENT, CAST REMOVAL, AC-POWERED

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-24
Device Publish Date2018-09-23

Devices Manufactured by STRYKER CORPORATION

07613327508437 - Tritanium X2024-09-16 TL Expandable Curved Posterior Lumbar Cage
07613327006933 - ES2 SPINAL SYSTEM2024-09-11 BLOCKER INSERTER
07613327006964 - ES2 SPINAL SYSTEM2024-09-11 ROD INSERTER
07613327006995 - ES2 SPINAL SYSTEM2024-09-11 RECOVERY GUIDE
07613327007008 - ES2 SPINAL SYSTEM2024-09-11 INNER SHAFT, RECOVERY SYSTEM
07613327007022 - ES2 SPINAL SYSTEM2024-09-11 THREADED RECOVERY GUIDE
07613327007046 - ES2 SPINAL SYSTEM2024-09-11 ROD INSERTER
07613327114867 - XIA 4.5 EVOLUTION2024-09-11 BLOCKER INSERTER

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.