Catalog Number

-

Brand Name

TMR Orthopedics Cannulated Screws

Version/Model Number

TMR 001-6.5-120

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K190830

Product Code

HWC

Product Code Name

Screw, Fixation, Bone

Public Device Record Key

e3c5d5bb-65e4-4289-b01d-4bcd6388896c

Public Version Date

October 17, 2022

Public Version Number

2

DI Record Publish Date

February 10, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-