Catalog Number

-

Brand Name

TiMesh®

Version/Model Number

015-102R

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

K062348

Product Code

HRS

Product Code Name

PLATE, FIXATION, BONE

Public Device Record Key

a77c8cc9-94c1-4311-83ec-d576172d445a

Public Version Date

February 05, 2021

Public Version Number

4

DI Record Publish Date

June 30, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-