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FLEXLITE CAMERA

Page Type
Cleared 510(K)
510(k) Number
K122134
510(k) Type
Traditional
Applicant
SPINE VIEW, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/2012
Days to Decision
162 days
Submission Type
Summary

FLEXLITE CAMERA

Page Type
Cleared 510(K)
510(k) Number
K122134
510(k) Type
Traditional
Applicant
SPINE VIEW, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/2012
Days to Decision
162 days
Submission Type
Summary