Duns Number:623316978
Device Description: Interbody Fusion Device 30 Degree 45 (M/L) 26 (A/P) 20 mm
Catalog Number
7130-2220-N
Brand Name
ENDOSKELETON® TL Hyperlordotic nanoLOCK® Surface Technology
Version/Model Number
7130-2220-N
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
December 23, 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
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
-
Product Code
OVD
Product Code Name
Intervertebral fusion device with integrated fixation, lumbar
Public Device Record Key
1ec99607-1a2b-4f16-98c4-53275b59d8cd
Public Version Date
October 21, 2022
Public Version Number
3
DI Record Publish Date
August 15, 2020
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 |