Ignite Creation Date:
2024-05-06 @ 9:45 AM
Last Modification Date:
2024-10-26 @ 12:19 PM
Study NCT ID:
NCT03062657
Status:
TERMINATED
Last Update Posted:
2024-04-05
First Post:
2017-02-20
Brief Title:
An Investigation of the Metal Concentration in Patients Implanted With the PRESTIGE LP Cervical Disc at Two Contiguous Levels in the Cervical Spine
Sponsor:
Medtronic Spinal and Biologics
Organization:
Medtronic Spinal and Biologics
Study Overview
Official Title:
An Investigation of the Metal Concentration in Patients Implanted With the PRESTIGE LP Cervical Disc at Two Contiguous Levels in the Cervical Spine
Status:
TERMINATED
Status Verified Date:
2024-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Study terminated prematurely as agreed by the FDA The FDA were satisfied that no further data was required despite the total number of patients who completed the study in full not being the agreed upon number
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This clinical study will assess the metal concentrations present in the blood serum of patients who receive surgical treatment with the PRESTIGE LP Cervical Disc at two contiguous cervical levels from C3-C7 The information obtained from this clinical investigation will be used to support the post market surveillance for a PMA supplement for the PRESTIGE LP Cervical Disc implanted at two contiguous levels
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
True
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
True
Is an FDA AA801 Violation?:
None