Sonoma Orthopedic Products, Inc - ARTHREX, INC.

Duns Number:131747628

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More Product Details

Catalog Number

CA4050

Brand Name

Sonoma Orthopedic Products, Inc

Version/Model Number

4.0mmx50mm Cancellous Bone Screw

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

July 07, 2020

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

-

Product Code Details

Product Code

HWC

Product Code Name

Screw, Fixation, Bone

Device Record Status

Public Device Record Key

47616f17-923c-4654-a779-253be915fd52

Public Version Date

July 08, 2020

Public Version Number

3

DI Record Publish Date

August 20, 2015

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ARTHREX, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 6506
2 A medical device with a moderate to high risk that requires special controls. 3411
3 A medical device with high risk that requires premarket approval 1
U Unclassified 2