SST Canulated Screws 9084.45.010

GUDID 08033390022668

Calibrated Kirschner Wire - SMR Shoulder

LIMACORPORATE SPA

Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable
Primary Device ID08033390022668
NIH Device Record Key1a10c8be-f619-440a-aecf-1eb7c73fc219
Commercial Distribution StatusIn Commercial Distribution
Brand NameSST Canulated Screws
Version Model NumberCalibrated Kirschner Wire
Catalog Number9084.45.010
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108033390022668 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWSProsthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08033390022668]

Moist Heat or Steam Sterilization


[08033390022668]

Moist Heat or Steam Sterilization


[08033390022668]

Moist Heat or Steam Sterilization


[08033390022668]

Moist Heat or Steam Sterilization


[08033390022668]

Moist Heat or Steam Sterilization


[08033390022668]

Moist Heat or Steam Sterilization


[08033390022668]

Moist Heat or Steam Sterilization


[08033390022668]

Moist Heat or Steam Sterilization


[08033390022668]

Moist Heat or Steam Sterilization


[08033390022668]

Moist Heat or Steam Sterilization


[08033390022668]

Moist Heat or Steam Sterilization


[08033390022668]

Moist Heat or Steam Sterilization


[08033390022668]

Moist Heat or Steam Sterilization


[08033390022668]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2023-05-03
Device Publish Date2016-08-05

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08033390260367 - PRIMA TT Glenoid2024-03-20 PRIMA TT Glenoid - Central Compressive Screw Cancellous Dia. 6,5 mm L. 20 mm
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