Last synced on 14 November 2025 at 11:06 pm

IntraLock System

Page Type
Cleared 510(K)
510(k) Number
K210159
510(k) Type
Traditional
Applicant
Fusion Orthopedics, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2021
Days to Decision
183 days
Submission Type
Summary

IntraLock System

Page Type
Cleared 510(K)
510(k) Number
K210159
510(k) Type
Traditional
Applicant
Fusion Orthopedics, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2021
Days to Decision
183 days
Submission Type
Summary