Last synced on 14 November 2025 at 11:06 pm

Navigated Spine Instruments

Page Type
Cleared 510(K)
510(k) Number
K203205
510(k) Type
Traditional
Applicant
Stryker Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/2021
Days to Decision
144 days
Submission Type
Summary

Navigated Spine Instruments

Page Type
Cleared 510(K)
510(k) Number
K203205
510(k) Type
Traditional
Applicant
Stryker Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/2021
Days to Decision
144 days
Submission Type
Summary