71931679

GUDID 00885556055458

MIS METAL OVAL PATELLA PROTECTOR 38MM

Smith & Nephew, Inc.

Surgical instrument guard, reusable

• Primary Device ID: 00885556055458
• NIH Device Record Key: 20b68d71-c9d2-4e87-ad77-fabc451f3765
• Commercial Distribution Discontinuation: 2016-07-03
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: 71931679
• Catalog Number: 71931679
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885556055458 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K121393

FDA Product Code

• HRY: PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER

Sterilization

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

[00885556055458]

Moist Heat or Steam Sterilization

[00885556055458]

Moist Heat or Steam Sterilization

[00885556055458]

Moist Heat or Steam Sterilization

[00885556055458]

Moist Heat or Steam Sterilization

[00885556055458]

Moist Heat or Steam Sterilization

[00885556055458]

Moist Heat or Steam Sterilization

[00885556055458]

Moist Heat or Steam Sterilization

[00885556055458]

Moist Heat or Steam Sterilization

[00885556055458]

Moist Heat or Steam Sterilization

[00885556055458]

Moist Heat or Steam Sterilization

[00885556055458]

Moist Heat or Steam Sterilization

[00885556055458]

Moist Heat or Steam Sterilization

[00885556055458]

Moist Heat or Steam Sterilization

[00885556055458]

Moist Heat or Steam Sterilization

[00885556055458]

Moist Heat or Steam Sterilization

[00885556055458]

Moist Heat or Steam Sterilization

[00885556055458]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-09-28

Devices Manufactured by Smith & Nephew, Inc.

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• 00885556901960 - EVOS: 2025-06-02 EVOS PELVIC 2.7MM X 26MM CORTEX SCREW BLUNT TIP
• 00885556901977 - EVOS: 2025-06-02 EVOS PELVIC 2.7MM X 28MM CORTEX SCREW BLUNT TIP
• 00885556901984 - EVOS: 2025-06-02 EVOS PELVIC 2.7MM X 30MM CORTEX SCREW BLUNT TIP
• 00885556901991 - EVOS: 2025-06-02 EVOS PELVIC 2.7MM X 32MM CORTEX SCREW BLUNT TIP
• 00885556902004 - EVOS: 2025-06-02 EVOS PELVIC 2.7MM X 34MM CORTEX SCREW BLUNT TIP
• 00885556902011 - EVOS: 2025-06-02 EVOS PELVIC 2.7MM X 36MM CORTEX SCREW BLUNT TIP
• 00885556902028 - EVOS: 2025-06-02 EVOS PELVIC 2.7MM X 38MM CORTEX SCREW BLUNT TIP