71932589

GUDID 00885556056165

SHORT TAPER STEM PC HO SIZE 7

Smith & Nephew, Inc.

Press-fit femoral stem prosthesis Press-fit femoral stem prosthesis Press-fit femoral stem prosthesis Press-fit femoral stem prosthesis Press-fit femoral stem prosthesis Press-fit femoral stem prosthesis Press-fit femoral stem prosthesis Press-fit femoral stem prosthesis Press-fit femoral stem prosthesis Press-fit femoral stem prosthesis Press-fit femoral stem prosthesis Press-fit femoral stem prosthesis Press-fit femoral stem prosthesis Press-fit femoral stem prosthesis Press-fit femoral stem prosthesis Press-fit femoral stem prosthesis Press-fit femoral stem prosthesis

• Primary Device ID: 00885556056165
• NIH Device Record Key: 1cd175d5-54c3-443a-b020-2ba7b41d54ec
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 71932589
• Catalog Number: 71932589
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885556056165 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K052792

FDA Product Code

• JDI: Prosthesis, hip, semi-constrained, metal/polymer, cemented

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-01-31
• Device Publish Date: 2015-08-29

Devices Manufactured by Smith & Nephew, Inc.

• 00885556747353 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 1 LEFT
• 00885556747360 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 2 LEFT
• 00885556747377 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 3 LEFT
• 00885556747384 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 5 LEFT
• 00885556747407 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 1 RIGHT
• 00885556747414 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 2 RIGHT
• 00885556747421 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 3 RIGHT
• 00885556747438 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 4 RIGHT