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SPINEFRONTIER LESPLASTY POSTERIOR CERVICAL LAMINOPLASTY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K132740
510(k) Type
Traditional
Applicant
SPINEFRONTIER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/2013
Days to Decision
84 days
Submission Type
Summary

SPINEFRONTIER LESPLASTY POSTERIOR CERVICAL LAMINOPLASTY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K132740
510(k) Type
Traditional
Applicant
SPINEFRONTIER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/2013
Days to Decision
84 days
Submission Type
Summary