Duns Number:295437313
Device Description: Corin BiPolar-i Ø41/22mm
Catalog Number
1110941
Brand Name
Corin BiPolar-i
Version/Model Number
1110941
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
K183114
Product Code
KWY
Product Code Name
Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
Public Device Record Key
cee4ced9-7c80-49f7-a2bd-a4e571d932b7
Public Version Date
September 09, 2020
Public Version Number
2
DI Record Publish Date
July 16, 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. | 3697 |
3 | A medical device with high risk that requires premarket approval | 21 |