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Biomet Fusion System

Page Type
Cleared 510(K)
510(k) Number
K163543
510(k) Type
Special
Applicant
Zimmer Biomet Spine Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2017
Days to Decision
74 days
Submission Type
Summary

Biomet Fusion System

Page Type
Cleared 510(K)
510(k) Number
K163543
510(k) Type
Special
Applicant
Zimmer Biomet Spine Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2017
Days to Decision
74 days
Submission Type
Summary