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LM BONE ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K960439
510(k) Type
Traditional
Applicant
LI MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/1996
Days to Decision
78 days
Submission Type
Summary

LM BONE ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K960439
510(k) Type
Traditional
Applicant
LI MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/1996
Days to Decision
78 days
Submission Type
Summary