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Clinical Trial

Stryker PEEK Customized Implant: A Prospective Post Market Follow Up to Evaluate Safety, Performance and Effectiveness

NCT: NCT05362370 · ACTIVE_NOT_RECRUITING

NCT IDNCT05362370
StatusACTIVE_NOT_RECRUITING
Start Date2023-02-01
Completion2027-06-30
SponsorStryker Craniomaxillofacial (INDUSTRY)
First posted
Last updated

Brief Summary

The purpose of this study is to confirm the safety, performance and effectiveness of Stryker's PEEK Customized Implants when used for the augmentation and/or restoration of bony and/or soft tissue deformities in the cranial and craniofacial skeleton. The study is designed as a prospective, multi-center trial with a long-term follow-up (up to 24-months) of study participants.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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