Duns Number:793384496
Device Description: ROD, PRE-BENT
Catalog Number
26-CC-PB-ROD-115
Brand Name
Streamline OCT Occipito-Cervico-Thoracic System
Version/Model Number
26-CC-PB-ROD-115
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
K172139
Product Code
KWP
Product Code Name
APPLIANCE, FIXATION, SPINAL INTERLAMINAL
Public Device Record Key
1aaddb49-e0da-40cf-b6c1-0924f5e64e97
Public Version Date
October 14, 2021
Public Version Number
2
DI Record Publish Date
December 16, 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 | 3116 |
2 | A medical device with a moderate to high risk that requires special controls. | 5221 |