Catalog Number

-

Brand Name

LOSPA TKR SYSTEM

Version/Model Number

KA.SPS.1320

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

-

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

K212034

Product Code

HWT

Product Code Name

Template

Public Device Record Key

c188dad5-783a-4f57-a0fb-74c8b0c226e3

Public Version Date

March 22, 2022

Public Version Number

2

DI Record Publish Date

December 31, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-