Catalog Number

-

Brand Name

Sofsilk

Version/Model Number

XX-5281

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

K981128,K981128

Product Code

GAP

Product Code Name

SUTURE, NONABSORBABLE, SILK

Public Device Record Key

885c0d54-c931-452c-b2c4-35be20bf6d3d

Public Version Date

May 03, 2022

Public Version Number

6

DI Record Publish Date

September 03, 2015

Package DI Number

20884521106052

Quantity per Package

36

Contains DI Package

10884521106055

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE