Catalog Number

SMARK-ATEC-2S-13-09

Brand Name

SecurMark for ATEC

Version/Model Number

SMARK-ATEC-2S-13-09

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K072913,K072913

Product Code

NEU

Product Code Name

MARKER, RADIOGRAPHIC, IMPLANTABLE

Public Device Record Key

fa78231d-d12e-49d0-9da0-ad93c349790d

Public Version Date

June 10, 2022

Public Version Number

4

DI Record Publish Date

August 29, 2015

Package DI Number

15420045503427

Quantity per Package

10

Contains DI Package

05420045503420

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX