Minima S Instrument Set 9045.03.208

GUDID 08033390153935

Trial Modular Neck #8

LIMACORPORATE SPA

Femoral stem prosthesis trial

• Primary Device ID: 08033390153935
• NIH Device Record Key: 37505b8f-605f-4a70-82fa-90c1f632d21b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Minima S Instrument Set
• Version Model Number: 9045.03.208
• Catalog Number: 9045.03.208
• Company DUNS: 432066322
• Company Name: LIMACORPORATE SPA
• 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: true
• OTC Over-The-Counter: false

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	08033390153935 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K141327

FDA Product Code

• MBL: Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous

Sterilization

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

[08033390153935]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-01-30
• Device Publish Date: 2020-01-22

On-Brand Devices [Minima S Instrument Set]

• 08033390084987: Trial Modular Neck #2
• 08033390084970: Trial Modular Neck #1
• 08033051091569: Trial Modular Neck #1 Lat.
• 08033390179317: Trial Modular Neck #1 Lat.
• 08033390153973: Trial Modular Neck #12
• 08033390153966: Trial Modular Neck #11
• 08033390153959: Trial Modular Neck #10
• 08033390153942: Trial Modular Neck #9
• 08033390153935: Trial Modular Neck #8
• 08033390153928: Trial Modular Neck #7