Guide Screw Set TKR.IN.1332

GUDID 14053613287668

Gebr. Brasseler GmbH & Co. KG

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• Primary Device ID: 14053613287668
• NIH Device Record Key: 67a608ee-4cc3-497e-9fac-5d376377c6bf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Guide Screw Set
• Version Model Number: TKR.IN.1332
• Catalog Number: TKR.IN.1332
• Company DUNS: 317409001
• Company Name: Gebr. Brasseler 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: 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 Identifiers

Device Issuing Agency	Device ID
GS1	14053613287668 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K131264

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: 2024-02-27
• Device Publish Date: 2024-02-19

On-Brand Devices [Guide Screw Set]

• 14053613287668: TKR.IN.1332
• 14053613287651: TKR.IN.1311
• 14053613287644: TKR.BB.1312