Aries-T Lumbar Interbody System 1150-3000

GUDID B06211503000

Aries TSLIF Inserter

Osseus Fusion Systems, LLC

Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable
Primary Device IDB06211503000
NIH Device Record Key556c3225-4735-418d-98a0-176fe7abd641
Commercial Distribution StatusIn Commercial Distribution
Brand NameAries-T Lumbar Interbody System
Version Model Number1150-3000
Catalog Number1150-3000
Company DUNS933442068
Company NameOsseus Fusion Systems, LLC
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
HIBCCB06211503000 [Primary]
HIBCCB06211503000 [Primary]
HIBCCB06211503000 [Primary]
HIBCCB06211503000 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FZXGuide, Surgical, Instrument
FZXGuide, Surgical, Instrument
FZXGuide, Surgical, Instrument
FZXGuide, Surgical, Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B06211503000]

Moist Heat or Steam Sterilization


[B06211503000]

Moist Heat or Steam Sterilization


[B06211503000]

Moist Heat or Steam Sterilization


[B06211503000]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-05-21
Device Publish Date2020-05-13

On-Brand Devices [Aries-T Lumbar Interbody System]

B0621150711010" Bone Funnel Impactor
B06211503000Aries TSLIF Inserter

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