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Reform® POCT System

Page Type
Cleared 510(K)
510(k) Number
K172495
510(k) Type
Traditional
Applicant
Precision Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/11/2018
Days to Decision
236 days
Submission Type
Summary

Reform® POCT System

Page Type
Cleared 510(K)
510(k) Number
K172495
510(k) Type
Traditional
Applicant
Precision Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/11/2018
Days to Decision
236 days
Submission Type
Summary