Duns Number:368715301
Device Description: RFS™ Screw Cannulated 4.5 x 50 mm
Catalog Number
RFS-C4550
Brand Name
RFS™ Screw
Version/Model Number
RFS-C4550
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
December 31, 2017
Issuing Agency
In HIBCC
MRI safety Status
MR Safe
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
K081392
Product Code
HWC
Product Code Name
Screw, Fixation, Bone
Public Device Record Key
98850f8e-111a-4c15-9701-2a388f3205ee
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
September 23, 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 | 142 |
2 | A medical device with a moderate to high risk that requires special controls. | 279 |