Duns Number:343548848
Device Description: Retractor, Spinal, quick-connect Lumbar-Blade 20x35mm SpineContr Retractor, Spinal, quick-connect Lumbar-Blade 20x35mm SpineControlâ„¢ Titanium (BLUE)
Catalog Number
29-3650.35
Brand Name
Retractor, Spinal, quick-connect Lumbar-Blade 20x35mm
Version/Model Number
29-3650.35
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"
Yes
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
GZT
Product Code Name
RETRACTOR, SELF-RETAINING, FOR NEUROSURGERY
Public Device Record Key
d790dcd6-137a-44c1-b951-1079f78e7d2e
Public Version Date
November 19, 2018
Public Version Number
1
DI Record Publish Date
October 18, 2018
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 |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 792 |