Duns Number:623316978
Device Description: Interbody Fusion Device Parallel Large 9mm
Catalog Number
5180-1609-N
Brand Name
ENDOSKELETON® TC nanoLOCK® Surface Technology
Version/Model Number
5180-1609-N
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
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
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
K100889,K141953
Product Code
ODP
Product Code Name
Intervertebral fusion device with bone graft, cervical
Public Device Record Key
868511ec-75a1-40b8-a910-4d433f8f00e0
Public Version Date
December 09, 2020
Public Version Number
6
DI Record Publish Date
December 15, 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 |
---|---|---|
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 |