Duns Number:424382307
Device Description: The Bilok® ST Screw is a cannulated, sterile, single-use bone screw made of an absorbable The Bilok® ST Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok® ST Screw is for use as a fixation screw in cruciate ligament surgery. It provides a combination of suspension and compression fixation that resorbs and it is subsequently replaced with bone during the healing process. Bilok® ST Screw is biodegradable and biocompatible.
Catalog Number
160-935ST
Brand Name
Bilok® ST Screw
Version/Model Number
160-935ST
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
January 02, 2020
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
-
Product Code
HWC
Product Code Name
Screw, Fixation, Bone
Public Device Record Key
11a07018-f836-414c-ad86-664dc8954b38
Public Version Date
November 02, 2020
Public Version Number
3
DI Record Publish Date
June 30, 2015
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 | 2 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 89 |