Catalog Number

60-70112

Brand Name

Paltop

Version/Model Number

60-70112

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

-

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

K112795

Product Code

DZI

Product Code Name

Drill, Bone, Powered

Public Device Record Key

d352aa41-fb2c-4974-8f9c-5e2b3a06ff63

Public Version Date

February 15, 2019

Public Version Number

4

DI Record Publish Date

December 04, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-