71933241

GUDID 00885556060599

SHORT TAPER STEM PC STD SIZE 4

Smith & Nephew, Inc.

Press-fit femoral stem prosthesis

• Primary Device ID: 00885556060599
• NIH Device Record Key: 7c988de5-d30b-44bf-be33-eca28ec09569
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 71933241
• Catalog Number: 71933241
• 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	00885556060599 [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.

• 00885556900567 - LEGION/GII: 2024-09-18 PATELLA CAPTURE ROUND/OVAL 29MM
• 00885556900574 - LEGION/GII: 2024-09-18 PATELLA CAPTURE ROUND/OVAL 32MM
• 00885556900581 - LEGION/GII: 2024-09-18 PATELLA CAPTURE ROUND/OVAL 35MM
• 00885556900598 - LEGION/GII: 2024-09-18 PATELLA CAPTURE ROUND/OVAL 38MM
• 00885556900604 - LEGION/GII: 2024-09-18 PATELLA CAPTURE ROUND/OVAL 41MM
• 00885556900611 - LEGION/GII: 2024-09-18 PATELLA CLAMP ATTACHMENT
• 00885556900628 - LEGION/GII: 2024-09-18 PATELLA SECONDARY SCREW CLAMP
• 00885556900635 - LEGION/GII: 2024-09-18 TIBIA REMOVAL TOOL