Duns Number:313267265
Device Description: TiAl6V4 ELI non-sterile
Catalog Number
FH30112
Brand Name
Merete® Cannulated PCS Compression Screw
Version/Model Number
3.0 12 Hex2.5
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
K090063,K120787
Product Code
HWC
Product Code Name
Screw, Fixation, Bone
Public Device Record Key
0134651e-3091-4303-b673-e54466f3b2bc
Public Version Date
August 01, 2018
Public Version Number
4
DI Record Publish Date
October 15, 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 | 328 |
2 | A medical device with a moderate to high risk that requires special controls. | 1327 |
U | Unclassified | 13 |