Trials / Withdrawn
WithdrawnNCT00858598
Pro Osteon Bone Void Filler Study
Pro Osteon Bone Void Filler Data Collection
- Status
- Withdrawn
- Phase
- —
- Study type
- Observational
- Enrollment
- 0 (actual)
- Sponsor
- Zimmer Biomet · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study was designed to observe the outcomes of Pro Osteon according to its cleared indications for use.
Detailed description
The purpose of this prospective clinical data-collection is to document the performance and clinical outcomes of Pro Osteon® as a Bone Void Filler. FDA has cleared this device via premarket notifications 510(k) K063346, K980817, and K990131. There will be no experimental or investigational devices used.
Conditions
Timeline
- Start date
- 2009-12-01
- Primary completion
- 2013-07-01
- Completion
- 2014-01-01
- First posted
- 2009-03-10
- Last updated
- 2017-06-21
Source: ClinicalTrials.gov record NCT00858598. Inclusion in this directory is not an endorsement.