Duns Number:623316978
Device Description: Trial, 7 Deg Lordotic, Large, 19mm
Catalog Number
2156-9219
Brand Name
ENDOSKELETON® TA VBR
Version/Model Number
2156-9219
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
September 18, 2020
Issuing Agency
In GS1
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
-
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
K032812
Product Code
MQP
Product Code Name
Spinal vertebral body replacement device
Public Device Record Key
3e70b81f-a22c-45e3-80d9-0eff857d1aa6
Public Version Date
December 09, 2020
Public Version Number
4
DI Record Publish Date
September 30, 2019
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 |
---|---|---|
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 |