Catalog Number

SCR4-13-05

Brand Name

Bioplate®

Version/Model Number

SCR4-13-05

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K953273,K953273

Product Code

JEY

Product Code Name

Plate, Bone

Public Device Record Key

6358303d-9a4a-49bc-abc9-3435754be7c5

Public Version Date

February 23, 2022

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

-