DYNALOK PLUS™ Spinal System - CONNECTOR 8436056C 6.35MM STRAIGHT - MEDTRONIC SOFAMOR DANEK, INC.

Duns Number:830350380

Device Description: CONNECTOR 8436056C 6.35MM STRAIGHT

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More Product Details

Catalog Number

-

Brand Name

DYNALOK PLUS™ Spinal System

Version/Model Number

8436056C

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

October 08, 2018

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

K991198

Product Code Details

Product Code

KWP

Product Code Name

APPLIANCE, FIXATION, SPINAL INTERLAMINAL

Device Record Status

Public Device Record Key

2956e2fc-36a0-4e4a-a368-b4a2ded2c53b

Public Version Date

February 06, 2019

Public Version Number

4

DI Record Publish Date

August 05, 2015

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"MEDTRONIC SOFAMOR DANEK, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 13352
2 A medical device with a moderate to high risk that requires special controls. 26085
3 A medical device with high risk that requires premarket approval 190
U Unclassified 75