Last synced on 14 November 2025 at 11:06 pm

OsteoCentric Bone Plate and Screw System

Page Type
Cleared 510(K)
510(k) Number
K190430
510(k) Type
Special
Applicant
OsteoCentric Trauma
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2019
Days to Decision
28 days
Submission Type
Summary

OsteoCentric Bone Plate and Screw System

Page Type
Cleared 510(K)
510(k) Number
K190430
510(k) Type
Special
Applicant
OsteoCentric Trauma
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2019
Days to Decision
28 days
Submission Type
Summary