A.L.P.S.MULTI-DIRECTIONAL LOCKING SCREW 856335014

GUDID 00887868062605

Biomet Orthopedics, LLC

Orthopaedic bone screw, non-bioabsorbable, sterile

• Primary Device ID: 00887868062605
• NIH Device Record Key: d3177844-69db-48b2-be2f-8491adf131ab
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: A.L.P.S.MULTI-DIRECTIONAL LOCKING SCREW
• Version Model Number: 8563-35-014
• Catalog Number: 856335014
• 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: 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)348-9500
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00887868062605 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K111663

FDA Product Code

• LXT: APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-10-24

On-Brand Devices [A.L.P.S.MULTI-DIRECTIONAL LOCKING SCREW]

• 00887868062834: 8563-35-060
• 00887868062827: 8563-35-058
• 00887868062810: 8563-35-056
• 00887868062803: 8563-35-054
• 00887868062797: 8563-35-052
• 00887868062780: 8563-35-050
• 00887868062773: 8563-35-048
• 00887868062766: 8563-35-046
• 00887868062759: 8563-35-044
• 00887868062742: 8563-35-042
• 00887868062735: 8563-35-040
• 00887868062728: 8563-35-038
• 00887868062711: 8563-35-036
• 00887868062704: 8563-35-034
• 00887868062698: 8563-35-032
• 00887868062681: 8563-35-030
• 00887868062674: 8563-35-028
• 00887868062667: 8563-35-026
• 00887868062650: 8563-35-024
• 00887868062643: 8563-35-022
• 00887868062636: 8563-35-020
• 00887868062629: 8563-35-018
• 00887868062612: 8563-35-016
• 00887868062605: 8563-35-014
• 00887868062599: 8563-35-012
• 00887868062582: 8563-35-010