Catalog Number

56-15904

Brand Name

UNIVERSAL NEURO 3

Version/Model Number

56-15904

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

K112557,K112557

Product Code

HBW

Product Code Name

FASTENER, PLATE, CRANIOPLASTY

Public Device Record Key

19333903-7f64-41d6-8d6c-45d3c1c3d35b

Public Version Date

July 01, 2019

Public Version Number

4

DI Record Publish Date

June 16, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-