Catalog Number

HTR-01-720221

Brand Name

CORVUS

Version/Model Number

HTR-01-720221

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K041936

Product Code

HWC

Product Code Name

Screw, Fixation, Bone

Public Device Record Key

a844abb8-a76a-46c8-8133-4e6b5b79d2cc

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

May 17, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-