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INTERMEDICS BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K850770
510(k) Type
Traditional
Applicant
INTERMEDICS ORTHOPEDICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/1985
Days to Decision
53 days

INTERMEDICS BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K850770
510(k) Type
Traditional
Applicant
INTERMEDICS ORTHOPEDICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/1985
Days to Decision
53 days