Catalog Number

1450-8501

Brand Name

Aries-L Lateral Lumbar Interbody System

Version/Model Number

1450-8501

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K181347

Product Code

MDM

Product Code Name

Instrument, Manual, Surgical, General Use

Public Device Record Key

16f146c2-a33e-4585-b3c4-7fe788ff6bd8

Public Version Date

August 20, 2020

Public Version Number

2

DI Record Publish Date

May 12, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-