BioStratis 2030SS

GUDID 10884521513310

Bio Absorbable ACL Soft Tissue Femoral Fixation Implant

Covidien LP

Meniscus screw

• Primary Device ID: 10884521513310
• NIH Device Record Key: ea0eb239-6590-484c-b255-533cf3b9727a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BioStratis
• Version Model Number: 2030SS
• Catalog Number: 2030SS
• Company DUNS: 058614483
• Company Name: Covidien LP
• 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(508)261-8000
• Email: covidien.udi@covidien.com

Device Dimensions

• Length: 25 Millimeter

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *

Device Identifiers

Device Issuing Agency	Device ID
GS1	10884521513310 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K041961

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: 4
• Public Version Date: 2019-06-07
• Device Publish Date: 2018-01-05

On-Brand Devices [BioStratis]

• 10884521513310: Bio Absorbable ACL Soft Tissue Femoral Fixation Implant
• 10884521513303: Bio Absorbable ACL Soft Tissue Femoral Fixation Implant
• 10884521513297: Bio Absorbable ACL Soft Tissue Femoral Fixation Implant