V-LoX3 10324T

GUDID M68510324T0

5.5mm V-LoX3 PEEK CF Suture Anchor

PARCUS MEDICAL LLC

Tendon/ligament bone anchor, non-bioabsorbable

• Primary Device ID: M68510324T0
• NIH Device Record Key: 94e0abc3-4cf8-4c08-9d7b-ad74182fe955
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: V-LoX3
• Version Model Number: 10324T
• Catalog Number: 10324T
• Company DUNS: 859961950
• Company Name: PARCUS MEDICAL LLC
• Device Count: 1
• DM Exempt: true
• 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: 941-755-7965
• Email: CustomerService@ParcusMedical.com

Device Dimensions

• Outer Diameter: 5.5 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M68510324T0 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K091094

FDA Product Code

• MBI: Fastener, Fixation, Nondegradable, Soft Tissue

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: 2019-07-03
• Device Publish Date: 2019-06-25

On-Brand Devices [V-LoX3]

• M68510325T0: 6.5mm V-LoX3 PEEK CF Suture Anchor
• M68510324T0: 5.5mm V-LoX3 PEEK CF Suture Anchor
• M68510358T0: 6.5mm V-LoX3 Titanium Suture Anchor
• M68510284T0: 5.5mm V-LoX3 Titanium Suture Anchor