ENDOSKELETON® TC nanoLOCK® Surface Technology - Interbody Fusion Device Parallel Large 9mm - TITAN SPINE, LLC

Duns Number:623316978

Device Description: Interbody Fusion Device Parallel Large 9mm

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More Product Details

Catalog Number

5180-1609-N

Brand Name

ENDOSKELETON® TC nanoLOCK® Surface Technology

Version/Model Number

5180-1609-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

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

K100889,K141953

Product Code Details

Product Code

ODP

Product Code Name

Intervertebral fusion device with bone graft, cervical

Device Record Status

Public Device Record Key

868511ec-75a1-40b8-a910-4d433f8f00e0

Public Version Date

December 09, 2020

Public Version Number

6

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