Catalog Number

-

Brand Name

ARVIS ®

Version/Model Number

11800

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

K203115

Product Code

OLO

Product Code Name

Orthopedic Stereotaxic Instrument

Public Device Record Key

8f6248ff-bca9-4b9d-b31d-14e218e1773c

Public Version Date

June 10, 2022

Public Version Number

2

DI Record Publish Date

November 12, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-