Catalog Number

PEEK-IM1004

Brand Name

Kelyniam CSI

Version/Model Number

PEEK-IM1004

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 08, 2021

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"

Yes

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

K103582

Product Code

GXN

Product Code Name

Plate, Cranioplasty, Preformed, Non-Alterable

Public Device Record Key

88f2111e-cc5d-495a-a031-8fa33726d1ee

Public Version Date

June 16, 2021

Public Version Number

1

DI Record Publish Date

June 08, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-