Duns Number:129278169
Catalog Number
IFI-491414
Brand Name
K-WIRE TROCAR POINT
Version/Model Number
IFI-491414
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
-
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
K110201,K110201
Product Code
HRS
Product Code Name
Plate, fixation, bone
Public Device Record Key
b1383667-1bdb-4780-b7b0-84e5b42a88c0
Public Version Date
April 07, 2020
Public Version Number
1
DI Record Publish Date
March 30, 2020
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 | 11962 |
2 | A medical device with a moderate to high risk that requires special controls. | 28376 |
3 | A medical device with high risk that requires premarket approval | 36 |
U | Unclassified | 4 |