Signature - SIG C/T TKA GDE/MDL SET 06-05 - Materialise NV

Duns Number:373139427

Device Description: SIG C/T TKA GDE/MDL SET 06-05

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More Product Details

Catalog Number

42-422771

Brand Name

Signature

Version/Model Number

42-422771

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

July 21, 2017

Issuing Agency

In HIBCC

Product Characteristics

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

K110415

Product Code Details

Product Code

HRY

Product Code Name

Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer

Device Record Status

Public Device Record Key

e55b5d46-8d64-47cf-9e17-828d5aad9734

Public Version Date

November 27, 2019

Public Version Number

4

DI Record Publish Date

September 24, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"MATERIALISE NV" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 91
2 A medical device with a moderate to high risk that requires special controls. 296