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ORTHOPEDIC IMPLANT SCREWS

Page Type
Cleared 510(K)
510(k) Number
K850024
510(k) Type
Traditional
Applicant
KIRKSTIL CORP., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/1985
Days to Decision
137 days

ORTHOPEDIC IMPLANT SCREWS

Page Type
Cleared 510(K)
510(k) Number
K850024
510(k) Type
Traditional
Applicant
KIRKSTIL CORP., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/1985
Days to Decision
137 days