TT MB Peg 1375.14.663

GUDID 08033390084437

SMR TT Metal Back Peg (Ti6Al4V) - S/STD Long

LIMACORPORATE SPA

Shoulder glenoid fossa prosthesis, prefabricated Shoulder glenoid fossa prosthesis, prefabricated Shoulder glenoid fossa prosthesis, prefabricated Shoulder glenoid fossa prosthesis, prefabricated Shoulder glenoid fossa prosthesis, prefabricated Shoulder glenoid fossa prosthesis, prefabricated Shoulder glenoid fossa prosthesis, prefabricated Shoulder glenoid fossa prosthesis, prefabricated Shoulder glenoid fossa prosthesis, prefabricated Shoulder glenoid fossa prosthesis, prefabricated Shoulder glenoid fossa prosthesis, prefabricated Shoulder glenoid fossa prosthesis, prefabricated Shoulder glenoid fossa prosthesis, prefabricated Shoulder glenoid fossa prosthesis, prefabricated Shoulder glenoid fossa prosthesis, prefabricated Shoulder glenoid fossa prosthesis, prefabricated Shoulder glenoid fossa prosthesis, prefabricated Shoulder glenoid fossa prosthesis, prefabricated

• Primary Device ID: 08033390084437
• NIH Device Record Key: 310bcbc5-36c8-4fd9-a15b-2ba2b619b01c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TT MB Peg
• Version Model Number: TT Glenoid
• Catalog Number: 1375.14.663
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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 Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	08033390084437 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K133349

FDA Product Code

• KWS: Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-12-23
• Device Publish Date: 2015-08-04

On-Brand Devices [TT MB Peg ]

• 08033390087902: SMR TT Metal Back Peg (Ti6Al4V) - S/STD X-Long
• 08033390087896: SMR TT Metal Back Peg (Ti6Al4V) - S-R X-Long
• 08033390084437: SMR TT Metal Back Peg (Ti6Al4V) - S/STD Long
• 08033390084420: SMR TT Metal Back Peg (Ti6Al4V) - S/STD Medium
• 08033390084413: SMR TT Metal Back Peg (Ti6Al4V) - S/STD Short
• 08033390084383: SMR TT Metal Back Peg (Ti6Al4V) - S-R Short