SMR TT Augmented 360 1375.15.557

GUDID 08033390180313

SMR TT Augmented 360 Baseplate S-R 7°X

LIMACORPORATE SPA

Shoulder glenoid fossa prosthesis, prefabricated
Primary Device ID08033390180313
NIH Device Record Key2b6baa3d-5433-4473-8d7e-fc50d317247b
Commercial Distribution StatusIn Commercial Distribution
Brand NameSMR TT Augmented 360
Version Model Number1375.15.557
Catalog Number1375.15.557
Company DUNS432066322
Company NameLIMACORPORATE SPA
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

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Device Identifiers

Device Issuing AgencyDevice ID
GS108033390180313 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

PHXShoulder Prosthesis, Reverse Configuration

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-12-07
Device Publish Date2020-11-27

On-Brand Devices [SMR TT Augmented 360]

08033390162104SMR TT Augmented 360 Baseplate S-R +4mm, Dia. 27 mm
08033390161848SMR TT Augmented 360 Baseplate S-R +2mm, Dia. 27 mm
08033390161473SMR TT Augmented 360 Baseplate S-R 15°, Dia. 27 mm
08033390161466SMR TT Augmented 360 Baseplate S-R 10°, Dia. 27 mm
08033390161459SMR TT Augmented 360 Baseplate S-R 7°, Dia. 27 mm
08033390180337SMR TT Augmented 360 Baseplate S-R 15°X
08033390180320SMR TT Augmented 360 Baseplate S-R 10°X
08033390180313SMR TT Augmented 360 Baseplate S-R 7°X
08033390180047SMR TT Augmented 360 Baseplate S-R 19°X
08033390161503SMR TT Augmented 360 Baseplate S-R 19°

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