Catalog Number

52-91766

Brand Name

AUTO PILOT

Version/Model Number

52-91766

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

K970912,K970912

Product Code

HWC

Product Code Name

Screw, fixation, bone

Public Device Record Key

a30f5e71-e69d-4eb9-813c-28c10e225864

Public Version Date

February 05, 2021

Public Version Number

4

DI Record Publish Date

December 03, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-