Catalog Number

29-56935

Brand Name

Universal Neuro 3

Version/Model Number

29-56935

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

K151387,K151387

Product Code

HBW

Product Code Name

FASTENER, PLATE, CRANIOPLASTY

Public Device Record Key

d89514eb-e9b9-406b-951f-d943a60296f6

Public Version Date

July 01, 2019

Public Version Number

4

DI Record Publish Date

September 24, 2015

Package DI Number

37613327090704

Quantity per Package

80

Contains DI Package

07613327090703

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

pack