Catalog Number

E0015886-1

Brand Name

Redapt

Version/Model Number

E0015886-1

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

K113789

Product Code

MEH

Product Code Name

Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate

Public Device Record Key

fe463257-4b85-4862-b892-9178e5f78099

Public Version Date

July 06, 2018

Public Version Number

2

DI Record Publish Date

March 07, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-