Duns Number:687844241
Device Description: 4CIS® Marlin PEEK ACIF Cage anatomical, Sterile, 12x12x7mm
Catalog Number
MPE0-C127
Brand Name
4CIS® Marlin ACIF Cage SYSTEM
Version/Model Number
MPE0-C127
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
December 28, 2018
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
K162402
Product Code
ODP
Product Code Name
Intervertebral Fusion Device With Bone Graft, Cervical
Public Device Record Key
47ed501d-dce3-47a6-9d11-cf986cd05fed
Public Version Date
March 28, 2022
Public Version Number
5
DI Record Publish Date
January 11, 2018
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 | 969 |
2 | A medical device with a moderate to high risk that requires special controls. | 6429 |