NAVIGATED XIA 3 48761330

GUDID 07613327064971

POLYAXIAL SCREWDRIVER

Stryker Corporation

General internal orthopaedic fixation system implantation kit
Primary Device ID07613327064971
NIH Device Record Keyc54bd6e9-db71-426f-84f8-1c58cc291b99
Commercial Distribution StatusIn Commercial Distribution
Brand NameNAVIGATED XIA 3
Version Model Number48761330
Catalog Number48761330
Company DUNS149183167
Company NameStryker Corporation
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS107613327064971 [Primary]

FDA Product Code

OLOOrthopedic stereotaxic instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07613327064971]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-09-24

On-Brand Devices [NAVIGATED XIA 3]

07613327065091TRAY
07613327065084MODULAR TAP
07613327065077MODULAR TAP
07613327065060MODULAR TAP
07613327065053MODULAR TAP
07613327065046MODULAR TAP
07613327065039MODULAR TAP
07613327065022THORACIC PEDICLE PROBE
07613327065015ROUND HANDLE RATCHET
07613327065008BLUNT PROBE
07613327064995CALIBRATION TIP
07613327064988T-HANDLE RATCHET
07613327064971POLYAXIAL SCREWDRIVER
07613327064964AWL

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