Duns Number:606417780
Device Description: Tag, 0 Degree ExtremiFuse, 2.4
Catalog Number
395-4001-24
Brand Name
OsteoMed
Version/Model Number
395-4001-24
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
-
Product Code
HWC
Product Code Name
Screw, fixation, bone
Public Device Record Key
4ce62ef2-2ab1-462b-b707-d47549357901
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
July 21, 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 | 95 |
2 | A medical device with a moderate to high risk that requires special controls. | 7762 |
U | Unclassified | 105 |