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BEAR® (Bridge-Enhanced ACL Restoration) Implant

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243578
510(k) Type
Traditional
Applicant
Miach Orthopaedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2025
Days to Decision
107 days
Submission Type
Summary

BEAR® (Bridge-Enhanced ACL Restoration) Implant

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243578
510(k) Type
Traditional
Applicant
Miach Orthopaedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2025
Days to Decision
107 days
Submission Type
Summary