IRB Study Number 26-627
Status Recruiting
Institute Neurological Institute
Description
- This is a prospective, multicenter observational registry to assess the clinical safety and performance of SYNTHECEL Dura Repair in subjects who undergo a cranial dura repair procedure.
Inclusion Criteria
- Subject aged 18 years or older at the time of consent.
- Subject or legally authorized representative who is willing to participate in the registry and provide written informed consent.
- Subject undergoing SYNTHECEL implantation for cranial dura repair on or after the start date of the registry study.
Exclusion Criteria
Subject with documented or known hypersensitivity or allergic reaction to cellulose or related materials.
