Catalog Number

CD-09-6200-S

Brand Name

HammerTech

Version/Model Number

CD-09-6200-S

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

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

K182684

Product Code

HWC

Product Code Name

Screw, Fixation, Bone

Public Device Record Key

42fd63dc-ae5c-4c7e-9bf1-eaab3f9db74a

Public Version Date

November 23, 2021

Public Version Number

2

DI Record Publish Date

April 29, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-