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Biomet Spine Fusion System

Page Type
Cleared 510(K)
510(k) Number
K151483
510(k) Type
Traditional
Applicant
Biomet Spine LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2015
Days to Decision
59 days
Submission Type
Summary

Biomet Spine Fusion System

Page Type
Cleared 510(K)
510(k) Number
K151483
510(k) Type
Traditional
Applicant
Biomet Spine LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2015
Days to Decision
59 days
Submission Type
Summary