MotionLoc™ NCB®

GUDID 00889024082700

Zimmer, Inc.

Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile

• Primary Device ID: 00889024082700
• NIH Device Record Key: 1265125c-3423-419c-8143-64f5351cb1f0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MotionLoc™ NCB®
• Version Model Number: 02.02161.040
• Company DUNS: 056038268
• Company Name: Zimmer, 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@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com

Device Dimensions

• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0
• Length: 40 Millimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024082700 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K101696

FDA Product Code

• HRS: PLATE, FIXATION, BONE

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: 2015-09-24

On-Brand Devices [MotionLoc™ NCB®]

• 00889024082922: 02.02162.046
• 00889024082915: 02.02162.044
• 00889024082908: 02.02162.042
• 00889024082892: 02.02162.040
• 00889024082885: 02.02162.038
• 00889024082878: 02.02162.036
• 00889024082861: 02.02162.034
• 00889024082854: 02.02162.032
• 00889024082847: 02.02162.030
• 00889024082830: 02.02162.028
• 00889024082823: 02.02162.026
• 00889024082816: 02.02162.024
• 00889024082809: 02.02161.060
• 00889024082793: 02.02161.058
• 00889024082786: 02.02161.056
• 00889024082779: 02.02161.054
• 00889024082762: 02.02161.052
• 00889024082755: 02.02161.050
• 00889024082748: 02.02161.048
• 00889024082731: 02.02161.046
• 00889024082724: 02.02161.044
• 00889024082717: 02.02161.042
• 00889024082700: 02.02161.040
• 00889024082694: 02.02161.038
• 00889024082687: 02.02161.036
• 00889024082670: 02.02161.034
• 00889024082663: 02.02161.032
• 00889024082656: 02.02161.030