Washer 6290-8-620

GUDID 07613327036176

Vitallium Washer for Bone Screw

Howmedica Osteonics Corp.

Orthopaedic bone washer, sterile Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer

• Primary Device ID: 07613327036176
• NIH Device Record Key: 792c4d11-6011-447d-b5c3-86e8c01c36c7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Washer
• Version Model Number: 6290-8-620
• Catalog Number: 6290-8-620
• Company DUNS: 058311945
• Company Name: Howmedica Osteonics Corp.
• 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

Device Dimensions

• Lumen/Inner Diameter: 6.2 Millimeter
• Lumen/Inner Diameter: 6.2 Millimeter
• Lumen/Inner Diameter: 6.2 Millimeter
• Lumen/Inner Diameter: 6.2 Millimeter
• Lumen/Inner Diameter: 6.2 Millimeter
• Lumen/Inner Diameter: 6.2 Millimeter
• Lumen/Inner Diameter: 6.2 Millimeter
• Lumen/Inner Diameter: 6.2 Millimeter
• Lumen/Inner Diameter: 6.2 Millimeter
• Lumen/Inner Diameter: 6.2 Millimeter
• Lumen/Inner Diameter: 6.2 Millimeter
• Lumen/Inner Diameter: 6.2 Millimeter
• Lumen/Inner Diameter: 6.2 Millimeter
• Lumen/Inner Diameter: 6.2 Millimeter
• Lumen/Inner Diameter: 6.2 Millimeter
• Lumen/Inner Diameter: 6.2 Millimeter
• Lumen/Inner Diameter: 6.2 Millimeter
• Lumen/Inner Diameter: 6.2 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327036176 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K864633

FDA Product Code

• HWC: Screw, 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

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