Catalog Number

PRO-1027-01

Brand Name

Navigated Spine Instruments

Version/Model Number

PRO-1027-01

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

K203205

Product Code

OLO

Product Code Name

Orthopedic stereotaxic instrument

Public Device Record Key

f0fa4228-bfb2-494e-a504-122724a12cf2

Public Version Date

January 13, 2022

Public Version Number

1

DI Record Publish Date

January 05, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-