Cannulated Lesser Hemi Implant

GUDID 00841731106414

CHI, Mini 13_Ti Bronze

VILEX IN TENNESSEE, INC.

Orthopaedic bone screw, non-bioabsorbable, non-sterile
Primary Device ID00841731106414
NIH Device Record Keycfb077cc-6c4d-45e0-9aee-9f0f333749e5
Commercial Distribution StatusIn Commercial Distribution
Brand NameCannulated Lesser Hemi Implant
Version Model NumberMCHI-13
Company DUNS152008371
Company NameVILEX IN TENNESSEE, INC.
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 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
GS100841731106414 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWDProsthesis, Toe, Hemi-, Phalangeal

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00841731106414]

Moist Heat or Steam Sterilization


[00841731106414]

Moist Heat or Steam Sterilization


[00841731106414]

Moist Heat or Steam Sterilization


[00841731106414]

Moist Heat or Steam Sterilization


[00841731106414]

Moist Heat or Steam Sterilization


[00841731106414]

Moist Heat or Steam Sterilization


[00841731106414]

Moist Heat or Steam Sterilization


[00841731106414]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-08-04

On-Brand Devices [Cannulated Lesser Hemi Implant]

00841731106414CHI, Mini 13_Ti Bronze
00841731106407CHI, Mini 12_Ti Green
00841731106391CHI, Mini 11_Ti Magenta
00841731106384CHI, Mini 10_Ti Gold
00841731106377CHI, Mini 09_Ti Blue

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.