Duns Number:129278169
Catalog Number
110027852
Brand Name
DISPOSABLE KIT W/ OSSEOTI IMPLANT
Version/Model Number
110027852
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Conditional
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
K151615
Product Code
JDR
Product Code Name
Staple, fixation, bone
Public Device Record Key
0c9fbf16-9965-4c44-b321-edcda04dea35
Public Version Date
November 23, 2021
Public Version Number
4
DI Record Publish Date
April 26, 2016
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 |