Catalog Number

1004459

Brand Name

Regensburg Type Total Titanium

Version/Model Number

1004459

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

K972585

Product Code

ETA

Product Code Name

Replacement, Ossicular Prosthesis, Total

Public Device Record Key

d1e97fae-be3b-4e8a-a765-a1e4c2f76f90

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 21, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-