Catalog Number

7601-N90010-M

Brand Name

Navigation Instruments

Version/Model Number

7601-N90010-M

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

Yes

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

K201006

Product Code

OLO

Product Code Name

Orthopedic stereotaxic instrument

Public Device Record Key

b0d0bd75-08a1-4a97-bb03-6d2bd607d8d4

Public Version Date

September 01, 2021

Public Version Number

2

DI Record Publish Date

October 29, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-