Catalog Number

-

Brand Name

Achilles EXPII

Version/Model Number

v1

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

K103633

Product Code

MUA

Product Code Name

Bone sonometer

Public Device Record Key

3936b9bc-1347-4b36-81d3-47032261b4e7

Public Version Date

February 12, 2020

Public Version Number

5

DI Record Publish Date

June 27, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-