Catalog Number

-

Brand Name

Titanium Elastic Nail

Version/Model Number

412-2.5-044

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

K192003

Product Code

JDS

Product Code Name

Nail, Fixation, Bone

Public Device Record Key

ac2de82d-0389-4c24-9b96-d5fd93bab8ba

Public Version Date

December 31, 2021

Public Version Number

1

DI Record Publish Date

December 23, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-