Duns Number:019936692
Device Description: VerteLP PEEK Implant
Catalog Number
VGLP22X65X97
Brand Name
VerteLP Interbody Fusion Device
Version/Model Number
VG-LP-22X65X9(7)
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
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
OVD
Product Code Name
Intervertebral Fusion Device With Integrated Fixation, Lumbar
Public Device Record Key
8161018f-789e-4fa0-8c8d-9188acb9556f
Public Version Date
February 24, 2020
Public Version Number
4
DI Record Publish Date
October 06, 2016
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 264 |