SOLIS 874009

GUDID 07613327262117

DISTRACTION PIN

Stryker Corporation

General internal orthopaedic fixation system implantation kit

• Primary Device ID: 07613327262117
• NIH Device Record Key: c8d79189-4fe9-49e7-a7b4-5aadb204d053
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SOLIS
• Version Model Number: 874009
• Catalog Number: 874009
• Company DUNS: 149183167
• Company Name: Stryker Corporation
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Length: 15 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327262117 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[07613327262117]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-10-25
• Device Publish Date: 2018-09-24

On-Brand Devices [SOLIS]

• 07613327262186: PIN GUIDE
• 07613327262131: DISTRACTION PIN
• 07613327262117: DISTRACTION PIN
• 07613327262063: PIN DRIVER
• 07613327141924: SPECIALTY AS INSERTER WITH STOP
• 07613327141870: SPECIALTY INSERTER WITH STOP