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MITEK BONE ANCHOR, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K915889
510(k) Type
Traditional
Applicant
MITEK SURGICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/1992
Days to Decision
307 days
Submission Type
Statement

MITEK BONE ANCHOR, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K915889
510(k) Type
Traditional
Applicant
MITEK SURGICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/1992
Days to Decision
307 days
Submission Type
Statement