Duns Number:832637081
Device Description: 13MM TI CANNULATED FEMORAL NAIL 400MM-STERILE
Catalog Number
474341S
Brand Name
NA
Version/Model Number
474.341S
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
September 01, 2019
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
K954856
Product Code
HTY
Product Code Name
PIN, FIXATION, SMOOTH
Public Device Record Key
21d7df04-2423-45b0-a4c2-5b6c6ecbb420
Public Version Date
September 02, 2019
Public Version Number
5
DI Record Publish Date
September 14, 2015
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 | 1194 |
2 | A medical device with a moderate to high risk that requires special controls. | 4171 |
3 | A medical device with high risk that requires premarket approval | 30 |
U | Unclassified | 1 |