Catalog Number

-

Brand Name

Remedy Spacer

Version/Model Number

RHSTMD

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

Yes

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K112470

Product Code

KWL

Product Code Name

Prosthesis, Hip, Hemi-, Femoral, Metal

Public Device Record Key

0a9e2b39-8132-4be2-bbaa-3a85218f6c35

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

April 06, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-