Catalog Number

-

Brand Name

Cirq Robotic Biopsy Guide Tube Cranial

Version/Model Number

56403

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

K210989

Product Code

HAW

Product Code Name

Neurological Stereotaxic Instrument

Public Device Record Key

6b8ca1c7-7303-427f-a99c-8df2b1290781

Public Version Date

December 02, 2021

Public Version Number

1

DI Record Publish Date

November 24, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-