Latarjet E0014839-5

GUDID 00885556646458

ANTERIOR GLENOID DRILL GUIDE - 6MM

Smith & Nephew, Inc.

Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable

• Primary Device ID: 00885556646458
• NIH Device Record Key: 8efd0564-520f-464d-a159-f4555b217b52
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Latarjet
• Version Model Number: E0014839-5
• Catalog Number: E0014839-5
• Company DUNS: 109903521
• Company Name: Smith & Nephew, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885556646458 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K121714

FDA Product Code

• HSD: PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

[00885556646458]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-11-22
• Device Publish Date: 2016-04-11

On-Brand Devices [Latarjet]

• 00885556716267: DIA. 15MM CANNULA COVER
• 00885556716250: DIA. 15MM CANNULA TUBE
• 00885556716243: DIA. 15MM CANNULA TROCAR
• 00885556708057: ARTHROSCOPIC LATARJET/BONE BLOCK LID
• 00885556708040: ARTHROSCOPIC LATARJET/BONE BLOCK TRAY
• 00885556708026: CORACOID DRILLING OFFSETGUIDE 10MM
• 00885556708019: CORACOID DRILLING GUIDE
• 00885556708002: SUBSCAP SPREADER SLIDING BLOCK
• 00885556707999: SUBSCAPULARIS SPREADER
• 00885556707982: SINGLE POSTERIOR GLENOID DRILL GUIDE
• 00885556707975: TISSUE RETRACTOR - 45 DEGREE
• 00885556707968: TISSUE RETRACTOR - 90 DEGREE
• 00885556707951: HALF CANNULA OBTURATOR - LONG
• 00885556707944: HALF CANNULA - LONG
• 00885556707791: SUTURE TENSIONER
• 00885556646489: OFFSET MEASUREMENT TOOL
• 00885556646472: ANTERIOR GLENOID DRILL GUIDE - 8MM
• 00885556646465: ANTERIOR GLENOID DRILL GUIDE - 7MM
• 00885556646458: ANTERIOR GLENOID DRILL GUIDE - 6MM
• 00885556646441: ANTERIOR GLENOID DRILL GUIDE - 5MM
• 00885556646434: CORACOID DRILL GUIDE 10MM OFFSET BLOCK
• 00885556646427: 5MM CORACOID DRILL GUIDE
• 00885556634196: BONE GRASPER
• 00885556746554: 9MM CIRCLE ANTERIOR DRILL GUIDE
• 00885556746547: 8MM CIRCLE ANTERIOR DRILL GUIDE
• 00885556746530: 7MM CIRCLE ANTERIOR DRILL GUIDE
• 00885556746509: 6MM CIRCLE ANTERIOR DRILL GUIDE
• 00885556746493: 9MM FORKED ANTERIOR DRILL GUIDE
• 00885556746479: 8MM FORKED ANTERIOR DRILL GUIDE
• 00885556746448: 7MM FORKED ANTERIOR DRILL GUIDE
• 00885556746431: 6MM FORKED ANTERIOR DRILL GUIDE
• 00885556746424: ADJUSTABLE GLENOID GUIDE