Catalog Number

72201991

Brand Name

OSTEORAPTOR / ULTRABRAID

Version/Model Number

72201991

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

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

K151105

Product Code

HWC

Product Code Name

Screw, fixation, bone

Public Device Record Key

7cc0a1e5-47cb-4887-be91-3611d6fb3079

Public Version Date

January 31, 2020

Public Version Number

6

DI Record Publish Date

September 21, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-