PERI-LOC System 71170496

GUDID 03596010638168

PERI-LOC LAT TIBIA BT TEMPLATE RIGHT FOR TITANIUM PLATE

Smith & Nephew, Inc.

General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit

• Primary Device ID: 03596010638168
• NIH Device Record Key: 1b928283-d0d2-48a5-872b-f3f518d66d36
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PERI-LOC System
• Version Model Number: 71170496
• Catalog Number: 71170496
• 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	03596010638168 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K123055

FDA Product Code

• HRS: Plate, fixation, bone

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-03-14
• Device Publish Date: 2022-03-04

On-Brand Devices [PERI-LOC System]

• 03596010638373: PERI-LOC L-D FEMUR TEMPLATE RIGHT FOR TITANIUM PLATE
• 03596010638359: PERI-LOC L-P TIBIA TEMPLATE RIGHT FOR TITANIUM PLATE
• 03596010638335: PERI-LOC A-L-D TIBIA TEMPLATE 3H RIGHT FOR TITANIUM PLATE
• 03596010638298: PERI-LOC M-D TIBIA TEMPLATE RIGHT FOR TITANIUM PLATE
• 03596010638274: PERI-LOC PROX HUMERUS TEMPLATE RIGHT FOR TITANIUM PLATE
• 03596010638250: PERI-LOC M-D HUMERUS TEMPLATE RIGHT FOR TITANIUM PLATE
• 03596010638243: PERI-LOC M-D HUMERUS TEMPLATE LEFT FOR TITANIUM PLATE
• 03596010638236: PERI-LOC P-L-D HUMERUS TEMPLATE RIGHT FOR TITANIUM PLATE
• 03596010638212: PERI-LOC L-D HUMERUS TEMPLATE RIGHT FOR TITANIUM PLATE
• 03596010638199: PERI-LOC OLECRANON TEMPLATE RIGHT FOR TITANIUM PLATE
• 03596010638151: PERI-LOC WIDE VDR TEMPLATE RIGHT FOR TITANIUM PLATE
• 03596010638137: PERI-LOC STD VDR TEMPLATE RIGHT FOR TITANIUM PLATE
• 03596010638168: PERI-LOC LAT TIBIA BT TEMPLATE RIGHT FOR TITANIUM PLATE