G7 PROVISIONAL NEUTRAL LINER 010002640

GUDID 00880304551794

Biomet Orthopedics, LLC

Acetabulum prosthesis trial, reusable Acetabulum prosthesis trial, reusable Acetabulum prosthesis trial, reusable Acetabulum prosthesis trial, reusable Acetabulum prosthesis trial, prefabricated, reusable Acetabulum prosthesis trial, prefabricated, reusable Acetabulum prosthesis trial, prefabricated, reusable Acetabulum prosthesis trial, prefabricated, reusable Acetabulum prosthesis trial, prefabricated, reusable Acetabulum prosthesis trial, prefabricated, reusable Acetabulum prosthesis trial, prefabricated, reusable Acetabulum prosthesis trial, prefabricated, reusable Acetabulum prosthesis trial, prefabricated, reusable Acetabulum prosthesis trial, prefabricated, reusable Acetabulum prosthesis trial, prefabricated, reusable Acetabulum prosthesis trial, prefabricated, reusable Acetabulum prosthesis trial, prefabricated, reusable Acetabulum prosthesis trial, prefabricated, reusable Acetabulum prosthesis trial, prefabricated, reusable

• Primary Device ID: 00880304551794
• NIH Device Record Key: 340bdac6-5b43-4bca-ac56-3b715b12aec1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: G7 PROVISIONAL NEUTRAL LINER
• Version Model Number: 010002640
• Catalog Number: 010002640
• 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
• 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 Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00880304551794 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K121874

FDA Product Code

• LZO: Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented

Sterilization

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

[00880304551794]

Moist Heat or Steam Sterilization

[00880304551794]

Moist Heat or Steam Sterilization

[00880304551794]

Moist Heat or Steam Sterilization

[00880304551794]

Moist Heat or Steam Sterilization

[00880304551794]

Moist Heat or Steam Sterilization

[00880304551794]

Moist Heat or Steam Sterilization

[00880304551794]

Moist Heat or Steam Sterilization

[00880304551794]

Moist Heat or Steam Sterilization

[00880304551794]

Moist Heat or Steam Sterilization

[00880304551794]

Moist Heat or Steam Sterilization

[00880304551794]

Moist Heat or Steam Sterilization

[00880304551794]

Moist Heat or Steam Sterilization

[00880304551794]

Moist Heat or Steam Sterilization

[00880304551794]

Moist Heat or Steam Sterilization

[00880304551794]

Moist Heat or Steam Sterilization

[00880304551794]

Moist Heat or Steam Sterilization

[00880304551794]

Moist Heat or Steam Sterilization

[00880304551794]

Moist Heat or Steam Sterilization

[00880304551794]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-02-07
• Device Publish Date: 2016-09-22

On-Brand Devices [G7 PROVISIONAL NEUTRAL LINER]

• 00880304565814: 010002644
• 00880304565807: 010002641
• 00880304565791: 010002636
• 00880304565784: 010002635
• 00880304565777: 010002634
• 00880304565760: 010002633
• 00880304565753: 010002632
• 00880304565746: 010002631
• 00880304565739: 010002630
• 00880304565722: 010002629
• 00880304565715: 010002628
• 00880304565708: 010002627
• 00880304565692: 010002626
• 00880304565685: 010002625
• 00880304565678: 010002624
• 00880304565616: 010002618
• 00880304551831: 010002643
• 00880304551824: 010002642
• 00880304551817: 010002637
• 00880304551800: 010002638
• 00880304551794: 010002640
• 00880304551787: 010002639