234-030-049

GUDID 04546540756619

UNIVERSAL WEDGE 10MM X 20MM (1.5MM BORE)

STRYKER CORPORATION

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)

• Primary Device ID: 04546540756619
• NIH Device Record Key: e986832e-42f7-4d9a-8914-1169dbd797e6
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 234-030-049
• Catalog Number: 234-030-049
• Company DUNS: 187502109
• Company Name: STRYKER CORPORATION
• 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: true
• 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(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx

Device Dimensions

• Lumen/Inner Diameter: 1.5 Millimeter
• Length: 20 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 1.5 Millimeter
• Length: 20 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 1.5 Millimeter
• Length: 20 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 1.5 Millimeter
• Length: 20 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 1.5 Millimeter
• Length: 20 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 1.5 Millimeter
• Length: 20 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 1.5 Millimeter
• Length: 20 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 1.5 Millimeter
• Length: 20 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 1.5 Millimeter
• Length: 20 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 1.5 Millimeter
• Length: 20 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 1.5 Millimeter
• Length: 20 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 1.5 Millimeter
• Length: 20 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 1.5 Millimeter
• Length: 20 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 1.5 Millimeter
• Length: 20 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 1.5 Millimeter
• Length: 20 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 1.5 Millimeter
• Length: 20 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 1.5 Millimeter
• Length: 20 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 1.5 Millimeter
• Length: 20 Millimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04546540756619 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K952460

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: 2015-09-09

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• 07613327261707 - OPUS: 2024-06-28 NUT WRENCH
• 07613327261714 - OPUS: 2024-06-28 SCREWDRIVER
• 07613327261721 - OPUS: 2024-06-28 ANTI-ROTATION WRENCH
• 07613327265132 - XIA PRECISION SYSTEM: 2024-06-28 XIA CANNULATED ROUND HANDLE RATCHET
• 07613327265170 - XIA PRECISION SYSTEM: 2024-06-28 XIA CANNULATED T-HANDLE NON-RATCHET
• 07613327265217 - XIA PRECISION SYSTEM: 2024-06-28 XIA CANNULATED ROUND HANDLE NON-RATCHET