Catalog Number

C0257

Brand Name

Ablation Platform Mounting Hardware

Version/Model Number

C0257-00733

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

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

K092192

Product Code

HAW

Product Code Name

Neurological stereotaxic Instrument

Public Device Record Key

5b2e78a2-092a-44b1-a0af-071999f9bb2a

Public Version Date

March 25, 2020

Public Version Number

1

DI Record Publish Date

March 17, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-