ENDOSKELETON® TAS nanoLOCK® Surface Technology - Interbody Fusion Device 12 Degree Hybrid 16mm - TITAN SPINE, LLC

Duns Number:623316978

Device Description: Interbody Fusion Device 12 Degree Hybrid 16mm

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More Product Details

Catalog Number

2312-1116-N

Brand Name

ENDOSKELETON® TAS nanoLOCK® Surface Technology

Version/Model Number

2312-1116-N

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

September 18, 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

K111626,K141953

Product Code Details

Product Code

OVD

Product Code Name

Intervertebral fusion device with integrated fixation, lumbar

Device Record Status

Public Device Record Key

99586e10-182a-4192-bdff-27c2877451ad

Public Version Date

December 09, 2020

Public Version Number

8

DI Record Publish Date

December 15, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"TITAN SPINE, LLC" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 243
2 A medical device with a moderate to high risk that requires special controls. 5255