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REVCON (TM) Screw System

Page Type
Cleared 510(K)
510(k) Number
K223392
510(k) Type
Traditional
Applicant
Voom Medical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2023
Days to Decision
112 days
Submission Type
Summary

REVCON (TM) Screw System

Page Type
Cleared 510(K)
510(k) Number
K223392
510(k) Type
Traditional
Applicant
Voom Medical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2023
Days to Decision
112 days
Submission Type
Summary