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Precision Spine Interspinous Plate System

Page Type
Cleared 510(K)
510(k) Number
K151863
510(k) Type
Special
Applicant
PRECISION SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/2015
Days to Decision
30 days
Submission Type
Summary

Precision Spine Interspinous Plate System

Page Type
Cleared 510(K)
510(k) Number
K151863
510(k) Type
Special
Applicant
PRECISION SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/2015
Days to Decision
30 days
Submission Type
Summary