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Biomet Spine Fusion System

Page Type
Cleared 510(K)
510(k) Number
K153695
510(k) Type
Special
Applicant
Biomet Spine LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/2016
Days to Decision
29 days
Submission Type
Summary

Biomet Spine Fusion System

Page Type
Cleared 510(K)
510(k) Number
K153695
510(k) Type
Special
Applicant
Biomet Spine LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/2016
Days to Decision
29 days
Submission Type
Summary