Catalog Number

915-9410

Brand Name

IQ LACTOSORB SYSTEM

Version/Model Number

915-9410

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

July 30, 2020

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

K955729

Product Code

HRS

Product Code Name

PLATE, FIXATION, BONE

Public Device Record Key

97d3fc2e-ca40-4055-aeb2-39dbc04fdb47

Public Version Date

July 31, 2020

Public Version Number

4

DI Record Publish Date

October 11, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-