Catalog Number

-

Brand Name

Oasis

Version/Model Number

MV-Y967

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

K130737,K130737,K130737

Product Code

GAM

Product Code Name

Suture, Absorbable, Synthetic, Polyglycolic Acid

Public Device Record Key

a42dbc5b-bd44-4bea-bf9b-c617856f53d9

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

January 14, 2016

Package DI Number

B031MVY9671

Quantity per Package

12

Contains DI Package

B031MVY9670

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-