Last synced on 23 September 2022 at 11:05 pm

Modified Trevo ProVue Retriever, Trevo XP ProVue Retriever 4x20mm, Trevo XP ProVue Retriever 3x20mm, Trevo XP ProVue Retriever 6x25mm, Trevo XP ProVue Retriever 4x30mm

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN150049
510(k) Type
Direct
Applicant
CONCENTRIC MEDICAL, INC.
Country
United States
FDA Decision
Deleted
Decision Date
9/2/2016
Days to Decision
312 days

Modified Trevo ProVue Retriever, Trevo XP ProVue Retriever 4x20mm, Trevo XP ProVue Retriever 3x20mm, Trevo XP ProVue Retriever 6x25mm, Trevo XP ProVue Retriever 4x30mm

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN150049
510(k) Type
Direct
Applicant
CONCENTRIC MEDICAL, INC.
Country
United States
FDA Decision
Deleted
Decision Date
9/2/2016
Days to Decision
312 days