SL-PLUS MIA 75001943

GUDID 07611996078893

SL-PLUS MIA STEM 5 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: 07611996078893
• NIH Device Record Key: ddf9cf7d-6276-4390-b583-e1a9b630923b
• Commercial Distribution Discontinuation: 2018-03-02
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: SL-PLUS MIA
• Version Model Number: 75001943
• Catalog Number: 75001943
• 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)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	07611996078893 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K082371

FDA Product Code

• KWY: Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or 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: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2015-08-29

On-Brand Devices [SL-PLUS MIA]

• 07611996079746: SL-PLUS MIA STEM LATERAL 12 NON-CEM
• 07611996079739: SL-PLUS MIA STEM LATERAL 11 NON-CEM
• 07611996079722: SL-PLUS MIA STEM LATERAL 10 NON-CEM
• 07611996079715: SL-PLUS MIA STEM LATERAL 9 NON-CEM
• 07611996079708: SL-PLUS MIA STEM LATERAL 8 NON-CEM
• 07611996079692: SL-PLUS MIA STEM LATERAL 7 NON-CEM
• 07611996079685: SL-PLUS MIA STEM LATERAL 6 NON-CEM
• 07611996079678: SL-PLUS MIA STEM LATERAL 5 NON-CEM
• 07611996079661: SL-PLUS MIA STEM LATERAL 4 NON-CEM
• 07611996079654: SL-PLUS MIA STEM LATERAL 3 NON-CEM
• 07611996079647: SL-PLUS MIA STEM LATERAL 2 NON-CEM
• 07611996079630: SL-PLUS MIA STEM LATERAL 1 NON-CEM
• 07611996079623: SL-PLUS MIA STEM 12 NON-CEM
• 07611996079616: SL-PLUS MIA STEM 11 NON-CEM
• 07611996079609: SL-PLUS MIA STEM 10 NON-CEM
• 07611996079593: SL-PLUS MIA STEM 9 NON-CEM
• 07611996079586: SL-PLUS MIA STEM 8 NON-CEM
• 07611996079579: SL-PLUS MIA STEM 1 NON-CEM
• 07611996079562: SL-PLUS MIA STEM 0 NON-CEM
• 07611996078916: SL-PLUS MIA STEM 7 NON-CEM
• 07611996078909: SL-PLUS MIA STEM 6 NON-CEM
• 07611996078893: SL-PLUS MIA STEM 5 NON-CEM
• 07611996078886: SL-PLUS MIA STEM 4 NON-CEM
• 07611996078879: SL-PLUS MIA STEM 3 NON-CEM
• 07611996078862: SL-PLUS MIA STEM 2 NON-CEM
• 07611996078855: SL-PLUS MIA STEM 01 NON-CEM