74033655

GUDID 03596010671851

UNIVERSAL INSERT SPACER SZ 5-6 15MM

Smith & Nephew, Inc.

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Primary Device ID03596010671851
NIH Device Record Key001fb316-288d-46df-9e6e-75aef367ed16
Commercial Distribution StatusIn Commercial Distribution
Version Model Number74033655
Catalog Number74033655
Company DUNS109903521
Company NameSmith & Nephew, Inc.
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 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)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM

Device Identifiers

Device Issuing AgencyDevice ID
GS103596010671851 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


[03596010671851]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2021-10-11
Device Publish Date2015-08-29

Devices Manufactured by Smith & Nephew, Inc.

00885556747353 - FASTPAK2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 1 LEFT
00885556747360 - FASTPAK2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 2 LEFT
00885556747377 - FASTPAK2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 3 LEFT
00885556747384 - FASTPAK2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 5 LEFT
00885556747407 - FASTPAK2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 1 RIGHT
00885556747414 - FASTPAK2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 2 RIGHT
00885556747421 - FASTPAK2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 3 RIGHT
00885556747438 - FASTPAK2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 4 RIGHT

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