Duns Number:435428396
Device Description: InterSpace Tapered Wedge Stem Trial XL is intended to be used for the selection of the rig InterSpace Tapered Wedge Stem Trial XL is intended to be used for the selection of the right size of InterSpace Tapered Wedge Stem XL to be implanted.
Catalog Number
-
Brand Name
InterSpace Tapered Wedge Stem Trial XL
Version/Model Number
SPC91Z3
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
-
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
HWT
Product Code Name
Template
Public Device Record Key
749aa79c-e206-418a-b36d-61aecd0e94c8
Public Version Date
October 03, 2022
Public Version Number
1
DI Record Publish Date
September 23, 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 | 37 |
2 | A medical device with a moderate to high risk that requires special controls. | 52 |