Duns Number:342615118
Device Description: BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operati BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
Catalog Number
BLP1030L00
Brand Name
BEE PLIF Cage
Version/Model Number
10 x 30 mm 0°
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
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
K211413
Product Code
MAX
Product Code Name
Intervertebral Fusion Device With Bone Graft, Lumbar
Public Device Record Key
2fd5c83c-0993-4174-8a0a-8076cb0ba4b9
Public Version Date
August 16, 2022
Public Version Number
1
DI Record Publish Date
August 08, 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 | 166 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 282 |