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ALLOFIX ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K053339
510(k) Type
Traditional
Applicant
Musculoskeletal Transplant Foundation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/2006
Days to Decision
105 days
Submission Type
Summary

ALLOFIX ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K053339
510(k) Type
Traditional
Applicant
Musculoskeletal Transplant Foundation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/2006
Days to Decision
105 days
Submission Type
Summary