Prestige LP Streamlined Instruments - TRIAL 6975247 TRIAL 7X14MM - MEDTRONIC SOFAMOR DANEK, INC.

Duns Number:830350380

Device Description: TRIAL 6975247 TRIAL 7X14MM

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More Product Details

Catalog Number

-

Brand Name

Prestige LP Streamlined Instruments

Version/Model Number

6975247

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

P090029

Product Code Details

Product Code

MJO

Product Code Name

Prosthesis, intervertebral disc

Device Record Status

Public Device Record Key

6281d874-4769-4a4e-a23e-ab00669a1f0b

Public Version Date

February 07, 2019

Public Version Number

4

DI Record Publish Date

February 11, 2018

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