TRYPTIK 2 C-PLATE INSTRUMENTATION - SCREWDRIVER T10 SOLID - SpineArt SA

Duns Number:483016148

Device Description: SCREWDRIVER T10 SOLID

Want to know more about this Product? Request more information now!


More Product Details

Catalog Number

TRY-IN 11 03-N

Brand Name

TRYPTIK 2 C-PLATE INSTRUMENTATION

Version/Model Number

TRY-IN 11 03-N

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

KWQ

Product Code Name

Appliance, Fixation, Spinal Intervertebral Body

Device Record Status

Public Device Record Key

24629773-7c1c-4d00-8994-e2432448ed1f

Public Version Date

March 04, 2019

Public Version Number

1

DI Record Publish Date

January 31, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"SPINEART SA" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 974
2 A medical device with a moderate to high risk that requires special controls. 5209