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ZESPIN SI Joint Fusion System, Paeon Posterior Cervical Fixation System, Paeon Anterior Cervical Plate System, Spinema Lumbar Plate System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221050
510(k) Type
Special
Applicant
Aegis Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2022
Days to Decision
80 days
Submission Type
Summary

ZESPIN SI Joint Fusion System, Paeon Posterior Cervical Fixation System, Paeon Anterior Cervical Plate System, Spinema Lumbar Plate System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221050
510(k) Type
Special
Applicant
Aegis Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2022
Days to Decision
80 days
Submission Type
Summary