OSSIO

GUDID B504OMTHN000570

Provision

Drilling power tool attachment, basic

• Primary Device ID: B504OMTHN000570
• NIH Device Record Key: 96aac65a-8a90-4bc8-93da-bdf491cb4313
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OSSIO
• Version Model Number: THN00057
• Company DUNS: 016889401
• Company Name: Provision
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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
HIBCC	B504OMTHN000570 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

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: 2024-02-22
• Device Publish Date: 2024-02-14

On-Brand Devices [OSSIO]

• B504OMTHN000570: THN00057
• B504OMOS7220350: OS722035
• B504OMOS7220270: OS722027
• B504OMOS7220240: OS722024
• B504OMOS7220190: OS722019