Catalog Number

ALL

Brand Name

OMT LLC

Version/Model Number

Pocket Pattie

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K020736,K020736

Product Code

HBA

Product Code Name

Neurosurgical Paddie

Public Device Record Key

d0003eec-79a3-476f-8ea3-1b8037ebe0dd

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

December 30, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-