Duns Number:033467608
Device Description: The Blustone Synergy Lumbar Interbody Fusion System (Basalt) may be implanted:- bi-lateral The Blustone Synergy Lumbar Interbody Fusion System (Basalt) may be implanted:- bi-laterally in pairs via a posterior (PLIF) approach;or,- as a single device via a transverse (T-PLIF) approach.
Catalog Number
-
Brand Name
Blustone Synergy Lumbar Interbody Fusion System (Basalt)
Version/Model Number
2410-PP08
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
K171893
Product Code
MAX
Product Code Name
Intervertebral Fusion Device With Bone Graft, Lumbar
Public Device Record Key
e09ba50e-1c06-4bdf-9f95-f94939d77b6f
Public Version Date
February 24, 2020
Public Version Number
4
DI Record Publish Date
January 29, 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 |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 76 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 64 |