NA - WORKSTATION 9731217 50901 CONFIGURED US - MEDTRONIC NAVIGATION, INC.

Duns Number:835233107

Device Description: WORKSTATION 9731217 50901 CONFIGURED US

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More Product Details

Catalog Number

-

Brand Name

NA

Version/Model Number

9731217

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

August 06, 2019

Issuing Agency

In GS1

Product Characteristics

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

-

Product Code Details

Product Code

HAW

Product Code Name

Neurological stereotaxic Instrument

Device Record Status

Public Device Record Key

25fdccd4-ae5a-4f39-95e6-2ee34d8354ac

Public Version Date

October 18, 2021

Public Version Number

3

DI Record Publish Date

September 19, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"MEDTRONIC NAVIGATION, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 23
2 A medical device with a moderate to high risk that requires special controls. 1961
3 A medical device with high risk that requires premarket approval 1