AIR+ 4722

GUDID 07613327482065

All-Inside Meniscal Repair System, Curved Up

STRYKER CORPORATION

Tendon/ligament bone anchor, non-bioabsorbable

• Primary Device ID: 07613327482065
• NIH Device Record Key: 886a734d-5967-42cb-a8b1-c8a904a63c78
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AIR+
• Version Model Number: 4722
• Catalog Number: 4722
• Company DUNS: 187502109
• Company Name: STRYKER CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	07613327482065 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K153087

FDA Product Code

• GAT: SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE

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: 2019-12-19
• Device Publish Date: 2019-12-11

On-Brand Devices [AIR+]

• 07613327499735: 2863-000-000
• 07613327482065: All-Inside Meniscal Repair System, Curved Up
• 07613327482072: All-Inside Meniscal Repair System, Curved Down