KOMET GUIDE PIN/SCREW - Gebr. Brasseler GmbH & Co. KG

Duns Number:317409001

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More Product Details

Catalog Number

GP005.067.032 STE

Brand Name

KOMET GUIDE PIN/SCREW

Version/Model Number

GP005.067.032.M5

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

K131264,K131264,K131264

Product Code Details

Product Code

HWC

Product Code Name

Screw, Fixation, Bone

Device Record Status

Public Device Record Key

4d72d971-dd9e-4b68-8943-60efb60b898b

Public Version Date

July 13, 2022

Public Version Number

2

DI Record Publish Date

December 18, 2020

Additional Identifiers

Package DI Number

24053613282066

Quantity per Package

1

Contains DI Package

14053613282069

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-

"GEBR. BRASSELER GMBH & CO. KG" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 154
2 A medical device with a moderate to high risk that requires special controls. 70