Catalog Number

-

Brand Name

Vertessa Lite 10x22cm

Version/Model Number

CAL-VL1022

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

K150016,K150016,K150016

Product Code

OTO

Product Code Name

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

Public Device Record Key

84671aa5-c159-49d5-99b4-19e8c8d43493

Public Version Date

July 19, 2022

Public Version Number

6

DI Record Publish Date

May 27, 2016

Package DI Number

00890594000643

Quantity per Package

1

Contains DI Package

00890594000339

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

box