92-51195

GUDID 07613154730575

BONE ANCHOR SCREWS,SELF-DRILLING

Stryker Leibinger GmbH & Co. KG

Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable

• Primary Device ID: 07613154730575
• NIH Device Record Key: 42d9980e-d3ef-492d-81cc-16496367bfb2
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 92-51195
• Catalog Number: 92-51195
• Company DUNS: 316153956
• Company Name: Stryker Leibinger GmbH & Co. KG
• 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: true
• 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

• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613154730575 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K041651

FDA Product Code

• DZE: IMPLANT, ENDOSSEOUS, ROOT-FORM

Sterilization

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

[07613154730575]

Moist Heat or Steam Sterilization

[07613154730575]

Moist Heat or Steam Sterilization

[07613154730575]

Moist Heat or Steam Sterilization

[07613154730575]

Moist Heat or Steam Sterilization

[07613154730575]

Moist Heat or Steam Sterilization

[07613154730575]

Moist Heat or Steam Sterilization

[07613154730575]

Moist Heat or Steam Sterilization

[07613154730575]

Moist Heat or Steam Sterilization

[07613154730575]

Moist Heat or Steam Sterilization

[07613154730575]

Moist Heat or Steam Sterilization

[07613154730575]

Moist Heat or Steam Sterilization

[07613154730575]

Moist Heat or Steam Sterilization

[07613154730575]

Moist Heat or Steam Sterilization

[07613154730575]

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: 2015-06-16

Devices Manufactured by Stryker Leibinger GmbH & Co. KG

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• 07613327556308 - NA: 2024-02-23 Facial iD MF 2 meshes
• 07613327556322 - NA: 2024-02-23 Facial iD MF 3 meshes
• 07613327556346 - NA: 2024-02-23 Facial iD MF 4 meshes
• 07613327556377 - NA: 2024-02-23 Facial iD MF 5 meshes
• 07613327556391 - NA: 2024-02-23 Facial iD MF 6 meshes
• 07613327556827 - NA: 2024-02-23 Facial iD MF 1 mesh kit