Duns Number:081021000
Device Description: LLIF IMPLANT - 0° x 22MM IMPLANTSLordosis & Heights: 14-17mm x 0° x 50mmCollapsed Width (m LLIF IMPLANT - 0° x 22MM IMPLANTSLordosis & Heights: 14-17mm x 0° x 50mmCollapsed Width (mm): 13.34Expanded Width (mm): 22Collapsed Height (mm): 14.5Expanded Height (mm): 17.5Collapsed Length (mm): 58.76Expanded Length (mm): 51.8LLIF SCREW - 50MM
Catalog Number
-
Brand Name
KIT DUALX LLIF 14-17MM x 0 DEG x 50MM
Version/Model Number
12833005023
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"
Yes
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
K181397
Product Code
MAX
Product Code Name
Intervertebral Fusion Device With Bone Graft, Lumbar
Public Device Record Key
972d0e1e-80a5-467e-87db-d52eaa04110c
Public Version Date
May 21, 2021
Public Version Number
5
DI Record Publish Date
May 13, 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 |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 277 |