Duns Number:042961576
Device Description: Caspar Type Compression/Distraction Device, 10 inch
Catalog Number
P99-150-0011LG
Brand Name
Baby Gorilla®/Gorilla® Plating System
Version/Model Number
P99-150-0011LG
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Unsafe
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
HWN
Product Code Name
INSTRUMENT, COMPRESSION
Public Device Record Key
d193903c-bb8d-42e3-ace2-7ad499dbebc0
Public Version Date
October 24, 2022
Public Version Number
1
DI Record Publish Date
October 14, 2022
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 | 1122 |
2 | A medical device with a moderate to high risk that requires special controls. | 3564 |