BRIDGE H PLATE, 6 HOLES, IMPLANT POSITIONER

GUDID 00888233069755

BIOMET MICROFIXATION, INC

Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool Orthopaedic fixation implant alignment tool

• Primary Device ID: 00888233069755
• NIH Device Record Key: a29bc1eb-d6d2-41d1-8254-80fd70e80d79
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BRIDGE H PLATE, 6 HOLES, IMPLANT POSITIONER
• Version Model Number: 215.202.06
• Company DUNS: 046189866
• Company Name: BIOMET MICROFIXATION, 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00888233069755 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K142484

FDA Product Code

• PBF: Orthopaedic Surgical Planning And Instrument Guides

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

[00888233069755]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-04-02
• Device Publish Date: 2024-03-25

Devices Manufactured by BIOMET MICROFIXATION, INC

• 00888233069373 - Sternalock EZ, Box Junction Plate, 10 Holes: 2024-04-02
• 00888233069380 - Sternalock EZ, O Junction Plate, 12 Holes: 2024-04-02
• 00888233069434 - Sternalock EZ, O Plate, 6 Holes: 2024-04-02
• 00888233069441 - 18mm Locking Screw: 2024-04-02
• 00888233069458 - 14mm Locking Screw: 2024-04-02
• 00888233069595 - Sternalock EZ, V Plate, 4 Holes: 2024-04-02
• 00888233069601 - Sternalock EZ, H Plate, 6 Holes: 2024-04-02
• 00888233069618 - Sternalock EZ, V Junction Plate, 10 Holes: 2024-04-02