VerteLP Interbody Fusion Device - VerteLP PEEK Implant - VGI MEDICAL, LLC

Duns Number:019936692

Device Description: VerteLP PEEK Implant

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More Product Details

Catalog Number

VGLP22X65X17

Brand Name

VerteLP Interbody Fusion Device

Version/Model Number

VG-LP-22X65X17

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

K151312

Product Code Details

Product Code

OVD

Product Code Name

Intervertebral Fusion Device With Integrated Fixation, Lumbar

Device Record Status

Public Device Record Key

c2f09c2d-4e21-4e24-9705-6d251098a7e3

Public Version Date

February 24, 2020

Public Version Number

4

DI Record Publish Date

October 04, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"VGI MEDICAL, LLC" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 264