Catalog Number

-

Brand Name

Ligament Staple

Version/Model Number

05.12.001

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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

K210456

Product Code

JDR

Product Code Name

Staple, Fixation, Bone

Public Device Record Key

d475de43-4393-4e42-9733-bf79fca06453

Public Version Date

November 23, 2021

Public Version Number

2

DI Record Publish Date

April 14, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-