'SLR-PLUS¿' 75001931

GUDID 07611996088304

SLR-PLUS REVISION STEM LATERAL 6 NON-CEM

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 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: 07611996088304
• NIH Device Record Key: 918c6d12-1e9c-48d1-b46c-c1804ff2a007
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 'SLR-PLUS¿'
• Version Model Number: 75001931
• Catalog Number: 75001931
• 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
• 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	07611996088304 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K093991

FDA Product Code

• LZO: Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-01-31
• Device Publish Date: 2015-08-29