MotionLoc® NCB®

GUDID 00889024083196

Zimmer, Inc.

Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

• Primary Device ID: 00889024083196
• NIH Device Record Key: 8b2f62c8-89f2-4985-84ed-8159fe96faa3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MotionLoc® NCB®
• Version Model Number: 02.03161.030
• 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: 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)348-2759
• 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

Device Dimensions

• Length: 30 Millimeter
• Device Size Text, specify: 0
• Length: 30 Millimeter
• Device Size Text, specify: 0
• Length: 30 Millimeter
• Device Size Text, specify: 0
• Length: 30 Millimeter
• Device Size Text, specify: 0
• Length: 30 Millimeter
• Device Size Text, specify: 0
• Length: 30 Millimeter
• Device Size Text, specify: 0
• Length: 30 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024083196 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K101696

FDA Product Code

• HWC: Screw, fixation, bone

Sterilization

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

[00889024083196]

Moist Heat or Steam Sterilization

[00889024083196]

Moist Heat or Steam Sterilization

[00889024083196]

Moist Heat or Steam Sterilization

[00889024083196]

Moist Heat or Steam Sterilization

[00889024083196]

Moist Heat or Steam Sterilization

[00889024083196]

Moist Heat or Steam Sterilization

[00889024083196]

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: 2017-09-26

On-Brand Devices [MotionLoc® NCB®]

• 00889024083462: 02.03162.046
• 00889024083455: 02.03162.044
• 00889024083448: 02.03162.042
• 00889024083431: 02.03162.040
• 00889024083424: 02.03162.038
• 00889024083417: 02.03162.036
• 00889024083400: 02.03162.034
• 00889024083394: 02.03162.032
• 00889024083387: 02.03162.030
• 00889024083370: 02.03162.028
• 00889024083363: 02.03162.026
• 00889024083356: 02.03162.024
• 00889024083349: 02.03161.060
• 00889024083332: 02.03161.058
• 00889024083325: 02.03161.056
• 00889024083318: 02.03161.054
• 00889024083301: 02.03161.052
• 00889024083295: 02.03161.050
• 00889024083288: 02.03161.048
• 00889024083271: 02.03161.046
• 00889024083264: 02.03161.044
• 00889024083257: 02.03161.042
• 00889024083240: 02.03161.040
• 00889024083233: 02.03161.038
• 00889024083226: 02.03161.036
• 00889024083219: 02.03161.034
• 00889024083202: 02.03161.032
• 00889024083196: 02.03161.030
• 00889024082335: 02.00024.999