THP™ HIP FRACTURE PLATING SYSTEMGUIDE SLEEVE, 5.0MM SCREW 14-451535

GUDID 00887868164644

Biomet Orthopedics, LLC

Orthopaedic implantation sleeve, reusable

• Primary Device ID: 00887868164644
• NIH Device Record Key: b66a9209-61c8-4f37-9ae3-296890da4a8e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: THP™ HIP FRACTURE PLATING SYSTEMGUIDE SLEEVE, 5.0MM SCREW
• Version Model Number: 14-451535
• Catalog Number: 14-451535
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• 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)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868164644 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K140018

FDA Product Code

• JDO: DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT

Sterilization

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

[00887868164644]

Moist Heat or Steam Sterilization

[00887868164644]

Moist Heat or Steam Sterilization

[00887868164644]

Moist Heat or Steam Sterilization

[00887868164644]

Moist Heat or Steam Sterilization

[00887868164644]

Moist Heat or Steam Sterilization

[00887868164644]

Moist Heat or Steam Sterilization

[00887868164644]

Moist Heat or Steam Sterilization

[00887868164644]

Moist Heat or Steam Sterilization

[00887868164644]

Moist Heat or Steam Sterilization

[00887868164644]

Moist Heat or Steam Sterilization

[00887868164644]

Moist Heat or Steam Sterilization

[00887868164644]

Moist Heat or Steam Sterilization

[00887868164644]

Moist Heat or Steam Sterilization

[00887868164644]

Moist Heat or Steam Sterilization

[00887868164644]

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: 2017-12-29

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• 00880304339224 - PARALLEL PULLER: 2024-09-11
• 00880304342187 - AGC MODULAR TIBIAL II: 2024-09-11
• 00880304365247 - BIO-MODULAR: 2024-09-11