Last synced on 30 May 2025 at 11:05 pm

Posterior Fusion Plate/HA Posterior Fusion Plate (Minuteman G1), Minuteman G3/HA Minuteman G3, HA Minuteman G3-R, Minuteman G5

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221023
510(k) Type
Traditional
Applicant
Spinal Simplicity LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2022
Days to Decision
135 days
Submission Type
Summary

Posterior Fusion Plate/HA Posterior Fusion Plate (Minuteman G1), Minuteman G3/HA Minuteman G3, HA Minuteman G3-R, Minuteman G5

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221023
510(k) Type
Traditional
Applicant
Spinal Simplicity LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2022
Days to Decision
135 days
Submission Type
Summary