Last synced on 14 November 2025 at 11:06 pm

Tigon Medical Gryphon Anchor Line

Page Type
Cleared 510(K)
510(k) Number
K220464
510(k) Type
Traditional
Applicant
Tigon Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2023
Days to Decision
398 days
Submission Type
Summary

Tigon Medical Gryphon Anchor Line

Page Type
Cleared 510(K)
510(k) Number
K220464
510(k) Type
Traditional
Applicant
Tigon Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2023
Days to Decision
398 days
Submission Type
Summary