TRIO TRAUMA 47113005

GUDID 04546540697387

PARALLEL DISTRACTOR

Stryker Corporation

Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable
Primary Device ID04546540697387
NIH Device Record Key83431c2d-3763-4340-94f0-9c2bfff0293b
Commercial Distribution StatusIn Commercial Distribution
Brand NameTRIO TRAUMA
Version Model Number47113005
Catalog Number47113005
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
GS104546540697387 [Primary]

FDA Product Code

NKBOrthosis, spinal pedicle fixation, for degenerative disc disease

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


[04546540697387]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-11-26
Device Publish Date2014-12-08

On-Brand Devices [TRIO TRAUMA]

07613252601012RAD ROD
07613252601005RAD ROD
07613252600992RAD ROD
07613252600985RAD ROD
07613252600978RAD ROD
07613252600961RAD ROD
07613252600954RAD ROD
07613252600947RAD ROD
07613252600930RAD ROD
07613252600916RAD ROD
07613252600909CANNULATED SCREW
07613252600893CANNULATED SCREW
07613252600886CANNULATED SCREW
07613252600879CANNULATED SCREW
07613252600862CANNULATED SCREW
04546540697493CUTTING PLIERS OUTER JAW
04546540697479CUTTING PLIERS INNER JAW
04546540697455CONNECTOR ADAPTOR
04546540697448OLIVE ADAPTOR
04546540697400KEY FOR PARALLEL DISTRACTOR
04546540697394CUTTING PLIERS
04546540697387PARALLEL DISTRACTOR
04546540697370TORQUE WRENCH TARGETING DEVICE
04546540683236CANNULATED SCREW
04546540683229CANNULATED SCREW
04546540683212CANNULATED SCREW
04546540683205CANNULATED SCREW
04546540683199CANNULATED SCREW
04546540683182CANNULATED SCREW
04546540683175CANNULATED SCREW
04546540683168CANNULATED SCREW
04546540683151CANNULATED SCREW
04546540683144CANNULATED SCREW
04546540683137CANNULATED SCREW
04546540680952STRAIGHT ROD
04546540680945STRAIGHT ROD
04546540680938STRAIGHT ROD
04546540680921STRAIGHT ROD
04546540680914STRAIGHT ROD
04546540680907STRAIGHT ROD
04546540680891STRAIGHT ROD
04546540680884STRAIGHT ROD
04546540680877STRAIGHT ROD
04546540680860STRAIGHT ROD
04546540680730RAD ROD
04546540680662CANNULATED SCREW
04546540680655CANNULATED SCREW
04546540680648CANNULATED SCREW
04546540680631CANNULATED SCREW
04546540680624CANNULATED SCREW

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