Catalog Number

-

Brand Name

INVISX™

Version/Model Number

60110

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

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

K010361,K010361

Product Code

GXN

Product Code Name

PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE

Public Device Record Key

f94be78c-d5c0-4f80-8741-982ca7f30ae4

Public Version Date

July 22, 2021

Public Version Number

4

DI Record Publish Date

July 16, 2015

Package DI Number

40643169496970

Quantity per Package

20

Contains DI Package

00643169496972

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CT