DISCOVERY - DISCOVERY SCREW SYSTEM CANNULATED FACET SCREW 4.0 - DEPUY SPINE, LLC

Duns Number:107105876

Device Description: DISCOVERY SCREW SYSTEM CANNULATED FACET SCREW 4.0 x 27.5mm

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More Product Details

Catalog Number

175703027

Brand Name

DISCOVERY

Version/Model Number

175703027

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

March 08, 2017

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

K012773

Product Code Details

Product Code

MRW

Product Code Name

SYSTEM, FACET SCREW SPINAL DEVICE

Device Record Status

Public Device Record Key

d9c75220-f7d7-48f8-a63b-0c7b98cf106a

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 24, 2015

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"DEPUY SPINE, LLC" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 5839
2 A medical device with a moderate to high risk that requires special controls. 2784
U Unclassified 20