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Biomet Fusion System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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