Titanium IntraLine 3910-400-065

GUDID 07613154890101

6.5MM TITANIUM INTRALINE ANCHOR WITH ¿ CIRCLE TAPER NEEDLES, 2 STRANDS #2 FORCE FIBER

STRYKER CORPORATION

Tendon/ligament bone anchor, non-bioabsorbable

• Primary Device ID: 07613154890101
• NIH Device Record Key: 3f12a19a-07df-497d-aebb-da0eb1d8729c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Titanium IntraLine
• Version Model Number: 3910-400-065
• Catalog Number: 3910-400-065
• 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

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613154890101 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K071157

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: 5
• Public Version Date: 2019-03-21
• Device Publish Date: 2015-09-04

On-Brand Devices [Titanium IntraLine]

• 07613154890101: 6.5MM TITANIUM INTRALINE ANCHOR WITH ¿ CIRCLE TAPER NEEDLES, 2 STRANDS #2 FORCE FIBER
• 07613154890095: 6.5MM TITANIUM INTRALINE ANCHOR WITH 2 STRANDS #2 FORCE FIBER
• 07613154890088: 5.5MM TITANIUM INTRALINE ANCHOR WITH 2 STRANDS #2 FORCE FIBER
• 07613154890071: 5.5MM TITANIUM INTRALINE ANCHOR WITH ¿ CIRCLE TAPER NEEDLES, 2 STRANDS #2 FORCE FIBER