MOSS MIAMI 174554999

GUDID 10705034019871

Moss Miami System SERRATED LAMINAR HOOK, WIDE 5mm

DEPUY SPINE, LLC

Bone-screw internal spinal fixation system, non-sterile

• Primary Device ID: 10705034019871
• NIH Device Record Key: 608046dc-0e7d-4065-aa90-5395dee3020d
• Commercial Distribution Discontinuation: 2019-05-31
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: MOSS MIAMI
• Version Model Number: 174554999
• Catalog Number: 174554999
• Company DUNS: 107105876
• Company Name: DEPUY SPINE, 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: 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)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10705034019871 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K933881

FDA Product Code

• KWP: APPLIANCE, FIXATION, SPINAL INTERLAMINAL

Sterilization

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

[10705034019871]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-05-31
• Device Publish Date: 2015-09-24

On-Brand Devices [MOSS MIAMI]

• 10705034033501: 5.5MM MOSS MIAMI SYSTEM PIN NUT 5.5mm
• 10705034019871: Moss Miami System SERRATED LAMINAR HOOK, WIDE 5mm