Duns Number:079700711
Device Description: Bone Staple
Catalog Number
-
Brand Name
NeoSpan™ SuperElastic Compression Staple w/Instruments, Size 25x22x22
Version/Model Number
T50 SN025
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
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
K161426
Product Code
JDR
Product Code Name
Staple, Fixation, Bone
Public Device Record Key
2f42d683-d005-4d2e-bc67-bb4d992c0b67
Public Version Date
November 23, 2021
Public Version Number
4
DI Record Publish Date
November 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 | 113 |
2 | A medical device with a moderate to high risk that requires special controls. | 1255 |