Duns Number:078812602
Device Description: Screw, Self Drilling, 4.6, Fixed
Catalog Number
0223-4511F
Brand Name
Cyclops Anterior Cervical Plate System
Version/Model Number
0223-4511F
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
K191786
Product Code
KWQ
Product Code Name
Appliance, fixation, spinal intervertebral body
Public Device Record Key
1f89229a-c9d8-4524-ba69-9fdd550fece4
Public Version Date
September 20, 2019
Public Version Number
1
DI Record Publish Date
September 12, 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 |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 511 |
2 | A medical device with a moderate to high risk that requires special controls. | 4143 |