GUDID 00889024305748

Orthosoft Inc

Orthopaedic prosthesis implantation instrument, single-use

• Primary Device ID: 00889024305748
• NIH Device Record Key: 68d370bb-89d0-4782-8669-0790566e2194
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 20-8070-009-00
• Company DUNS: 205670032
• Company Name: Orthosoft 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)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: 1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: 1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: 1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: 1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: 1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: 1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: 1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: 1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: 1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: 1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: 1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: 1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: 1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: 1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024305748 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K131409

FDA Product Code

• OOG: Knee Arthroplasty Implantation System

Sterilization

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

[00889024305748]

Moist Heat or Steam Sterilization

[00889024305748]

Moist Heat or Steam Sterilization

[00889024305748]

Moist Heat or Steam Sterilization

[00889024305748]

Moist Heat or Steam Sterilization

[00889024305748]

Moist Heat or Steam Sterilization

[00889024305748]

Moist Heat or Steam Sterilization

[00889024305748]

Moist Heat or Steam Sterilization

[00889024305748]

Moist Heat or Steam Sterilization

[00889024305748]

Moist Heat or Steam Sterilization

[00889024305748]

Moist Heat or Steam Sterilization

[00889024305748]

Moist Heat or Steam Sterilization

[00889024305748]

Moist Heat or Steam Sterilization

[00889024305748]

Moist Heat or Steam Sterilization

[00889024305748]

Moist Heat or Steam Sterilization

[00889024305748]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-02-07
• Device Publish Date: 2017-06-13

Devices Manufactured by Orthosoft Inc

• 00887868578915 - HAMMR™: 2024-05-01
• 00887868557873 - ROSA® Shoulder: 2024-03-14
• 00887868557880 - ROSA® Shoulder: 2024-03-14
• 00887868557897 - ROSA® Shoulder: 2024-03-14
• 00887868557903 - ROSA® Shoulder: 2024-03-14
• 00887868557910 - ROSA® Shoulder: 2024-03-14
• 00887868558078 - ROSA® Shoulder: 2024-03-14
• 00887868558092 - ROSA® Shoulder: 2024-03-14