Catalog Number

95512

Brand Name

SERI Contour

Version/Model Number

95512

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

MRI safety Status

MR Safe

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

K172545

Product Code

OXF

Product Code Name

Mesh, Surgical, Absorbable, Plastic And Reconstructive Surgery

Public Device Record Key

4cbbc922-0130-4d4c-9def-9ca0023e1a15

Public Version Date

June 10, 2022

Public Version Number

3

DI Record Publish Date

March 08, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-