H Plate, 6 Holes Provisional

GUDID 00851599007761

JACE MEDICAL, LLC

Spinal implant trial

• Primary Device ID: 00851599007761
• NIH Device Record Key: 39ac09c6-fd33-431f-8961-a6776b10731a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: H Plate, 6 Holes Provisional
• Version Model Number: 215.112.06
• Company DUNS: 063554875
• Company Name: JACE MEDICAL, LLC
• 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	00851599007761 [Primary]

FDA Product Code

• PBF: Orthopaedic Surgical Planning And Instrument Guides

Sterilization

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

[00851599007761]

Moist Heat or Steam Sterilization

[00851599007761]

Moist Heat or Steam Sterilization

[00851599007761]

Moist Heat or Steam Sterilization

[00851599007761]

Moist Heat or Steam Sterilization

[00851599007761]

Moist Heat or Steam Sterilization

[00851599007761]

Moist Heat or Steam Sterilization

[00851599007761]

Moist Heat or Steam Sterilization

[00851599007761]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-02-07
• Device Publish Date: 2018-01-26

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