AxTiHA® - Ti 6Al 4V (ELI); Hydroxyapatite - Innovasis, Inc.

Duns Number:156567492

Device Description: Ti 6Al 4V (ELI); Hydroxyapatite

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More Product Details

Catalog Number

AXTi144014

Brand Name

AxTiHA®

Version/Model Number

AXTi144014

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

K182139,K201614,K182139,K201614

Product Code Details

Product Code

OVD

Product Code Name

Intervertebral Fusion Device With Integrated Fixation, Lumbar

Device Record Status

Public Device Record Key

b4450b42-440b-44d0-bf02-19df05cd3194

Public Version Date

August 31, 2021

Public Version Number

3

DI Record Publish Date

August 31, 2019

Additional Identifiers

Package DI Number

M711AXTI1440141

Quantity per Package

1

Contains DI Package

M711AXTI1440140

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton

"INNOVASIS, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 252
2 A medical device with a moderate to high risk that requires special controls. 2102