TOE JOINT TITANIUM PC MD 20MM

GUDID 00810012480246

BIOPRO, INC.

Partial metatarsophalangeal joint prosthesis

• Primary Device ID: 00810012480246
• NIH Device Record Key: 9a44d018-87a2-4385-bbcf-58a427c1adad
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TOE JOINT TITANIUM PC MD 20MM
• Version Model Number: 17036
• Company DUNS: 618749857
• Company Name: BIOPRO, INC.
• 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: true
• Expiration Date: false
• 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
GS1	00810012480246 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K041595

FDA Product Code

• KWD: Prosthesis, Toe, Hemi-, Phalangeal

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: 2019-06-14
• Device Publish Date: 2019-06-06

On-Brand Devices [TOE JOINT TITANIUM PC MD 20MM]

• 00810012480246: 17036
• M209170360: 17036