Catalog Number

BMS-050RC

Brand Name

BioSphere MIS

Version/Model Number

Replacement Cannula

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

K173301

Product Code

MQV

Product Code Name

Filler, Bone Void, Calcium Compound

Public Device Record Key

4a470cf4-1b8f-4973-890e-f37a061e7eb4

Public Version Date

June 19, 2020

Public Version Number

4

DI Record Publish Date

February 12, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-