MEDPOR CONTAIN 81067

GUDID 07613252084488

MEDPOR¿ CONTAIN? Implant Sheet

Stryker Leibinger GmbH & Co. KG

Synthetic bone graft Synthetic bone graft Synthetic bone graft Synthetic bone graft Synthetic bone graft Synthetic bone graft Synthetic bone graft Synthetic bone graft Synthetic bone graft Synthetic bone graft Synthetic bone graft Synthetic bone graft Synthetic bone graft Synthetic bone graft Synthetic bone graft

• Primary Device ID: 07613252084488
• NIH Device Record Key: 64ef9316-0fa7-43f1-83a8-5d1da181de90
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MEDPOR CONTAIN
• Version Model Number: 81067
• Catalog Number: 81067
• Company DUNS: 316153956
• Company Name: Stryker Leibinger GmbH & Co. KG
• Device Count: 1
• DM Exempt: true
• 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: true
• 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

Device Dimensions

• Width: 25 Millimeter
• Length: 30 Millimeter
• Device Size Text, specify: 0
• Width: 25 Millimeter
• Length: 30 Millimeter
• Device Size Text, specify: 0
• Width: 25 Millimeter
• Length: 30 Millimeter
• Device Size Text, specify: 0
• Width: 25 Millimeter
• Length: 30 Millimeter
• Device Size Text, specify: 0
• Width: 25 Millimeter
• Length: 30 Millimeter
• Device Size Text, specify: 0
• Width: 25 Millimeter
• Length: 30 Millimeter
• Device Size Text, specify: 0
• Width: 25 Millimeter
• Length: 30 Millimeter
• Device Size Text, specify: 0
• Width: 25 Millimeter
• Length: 30 Millimeter
• Device Size Text, specify: 0
• Width: 25 Millimeter
• Length: 30 Millimeter
• Device Size Text, specify: 0
• Width: 25 Millimeter
• Length: 30 Millimeter
• Device Size Text, specify: 0
• Width: 25 Millimeter
• Length: 30 Millimeter
• Device Size Text, specify: 0
• Width: 25 Millimeter
• Length: 30 Millimeter
• Device Size Text, specify: 0
• Width: 25 Millimeter
• Length: 30 Millimeter
• Device Size Text, specify: 0
• Width: 25 Millimeter
• Length: 30 Millimeter
• Device Size Text, specify: 0
• Width: 25 Millimeter
• Length: 30 Millimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613252084488 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K091120

FDA Product Code

• NPK: Barrier, synthetic, intraoral

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2015-09-24

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