Duns Number:488227125
Device Description: Posterior Interbody Fusion Device 11x22x8 L5°
Catalog Number
-
Brand Name
Mectalif Posterior
Version/Model Number
03.27.033
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
K133192
Product Code
MAX
Product Code Name
Intervertebral Fusion Device With Bone Graft, Lumbar
Public Device Record Key
4e2d709e-129d-40da-8476-bb4219945bf5
Public Version Date
February 24, 2020
Public Version Number
4
DI Record Publish Date
November 18, 2014
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 | 8200 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 9084 |