Catalog Number

-

Brand Name

Vertessa Lite Y-Mesh 26x5x4cm

Version/Model Number

CAL-VLY2654

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

K150023,K150023,K150023

Product Code

OTO

Product Code Name

Mesh, Surgical, Synthetic, Urogynecologic, For Apical Vaginal And Uterine Prolapse, Transabdominally Placed

Public Device Record Key

a25075dc-60c6-4a20-95bb-15ed17844a52

Public Version Date

July 19, 2022

Public Version Number

7

DI Record Publish Date

October 30, 2015

Package DI Number

00890594000773

Quantity per Package

3

Contains DI Package

00890594000797

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box