Catalog Number

66-WP-AN1

Brand Name

WayPoint™ Anchors

Version/Model Number

66-WP-AN1-00623

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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,K092192

Product Code

HAW

Product Code Name

Neurological stereotaxic Instrument

Public Device Record Key

54b9d281-2e1e-4605-aeaf-66bf3a82a45c

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

October 16, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-