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/ Centermed, Inc.
Centermed, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K211614
CenterMed Patient Matched Assisted Surgical Planning (ASP) System
August 4, 2022
K201353
CenterMed Patient Matched Assisted Surgical Planning (ASP) System
June 28, 2021