INCITE INNOVATION ANCHORED CERVICAL INERBODY DEVICE - ANCHORED CERVICAL INTERBODY DEVICE, 8MM IMPLANT, - INCITE INNOVATION

Duns Number:005840144

Device Description: ANCHORED CERVICAL INTERBODY DEVICE, 8MM IMPLANT, 12x14MM, 5 DEGREE

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More Product Details

Catalog Number

22-9223

Brand Name

INCITE INNOVATION ANCHORED CERVICAL INERBODY DEVICE

Version/Model Number

22-9223

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K122008

Product Code Details

Product Code

OVE

Product Code Name

Intervertebral Fusion Device With Integrated Fixation, Cervical

Device Record Status

Public Device Record Key

6f041575-737d-48fc-aac7-6a4b231072e1

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

October 22, 2015

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"INCITE INNOVATION" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 26