Humelock II Cemented Shoulder System - K-WIRE CENTER GUIDE Ø43 mm - FX SOLUTIONS

Duns Number:263076196

Device Description: K-WIRE CENTER GUIDE Ø43 mm

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More Product Details

Catalog Number

902-0143

Brand Name

Humelock II Cemented Shoulder System

Version/Model Number

902-0143

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

-

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

-

Product Code Details

Product Code

FZX

Product Code Name

Guide, Surgical, Instrument

Device Record Status

Public Device Record Key

e7809feb-8dad-4dcb-a888-6b140f3e3c2c

Public Version Date

October 07, 2021

Public Version Number

2

DI Record Publish Date

September 27, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"FX SOLUTIONS" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 663
2 A medical device with a moderate to high risk that requires special controls. 478