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RELIEVE LAMINOPLASTY FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K080664
510(k) Type
Traditional
Applicant
GLOBUS MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2008
Days to Decision
137 days
Submission Type
Summary

RELIEVE LAMINOPLASTY FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K080664
510(k) Type
Traditional
Applicant
GLOBUS MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2008
Days to Decision
137 days
Submission Type
Summary