Duns Number:001403807
Device Description: UNIVERSAL KNEE SPLINT
Catalog Number
-
Brand Name
E.M Adams co, inc.
Version/Model Number
3030
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
June 21, 2021
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)
Yes
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
-
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
HSP
Product Code Name
Splint, Traction
Public Device Record Key
e4d448d8-7f5d-45bd-9112-38d96639a2c0
Public Version Date
June 22, 2021
Public Version Number
2
DI Record Publish Date
December 31, 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 |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 1447 |
2 | A medical device with a moderate to high risk that requires special controls. | 11 |