IMN Screws 2361-4060S

GUDID 07613327400557

Advanced Locking Screw

Stryker Trauma GmbH

Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw, non-bioabsorbable, sterile Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding)

• Primary Device ID: 07613327400557
• NIH Device Record Key: a6d74786-7f45-4e12-a9e0-e35d60e0e547
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IMN Screws
• Version Model Number: 2361-4060S
• Catalog Number: 2361-4060S
• Company DUNS: 330211587
• Company Name: Stryker Trauma GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: 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

• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter
• Device Size Text, specify: 0
• Length: 60 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327400557 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K193308

FDA Product Code

• HWC: Screw, fixation, bone

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-03-11
• Device Publish Date: 2020-03-03

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• 07613327400618: Advanced Locking Screw
• 07613327400601: Advanced Locking Screw
• 07613327400595: Advanced Locking Screw
• 07613327400588: Advanced Locking Screw
• 07613327400571: Advanced Locking Screw
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• 07613327400540: Advanced Locking Screw
• 07613327400533: Advanced Locking Screw
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• 07613327364903: Locking Screw