Catalog Number

-

Brand Name

PRECISE CENTERED PARTIAL 0.5MM L

Version/Model Number

765-050

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

K061853

Product Code

ETB

Product Code Name

Prosthesis, Partial Ossicular Replacement

Public Device Record Key

5d2777a6-6169-4c51-968b-3c68c0cdc382

Public Version Date

July 13, 2020

Public Version Number

2

DI Record Publish Date

October 05, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-