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STEREOTACTIC BODY FRAME

Page Type
Cleared 510(K)
510(k) Number
K960338
510(k) Type
Traditional
Applicant
ELEKTA INSTRUMENT AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/1996
Days to Decision
90 days
Submission Type
Summary

STEREOTACTIC BODY FRAME

Page Type
Cleared 510(K)
510(k) Number
K960338
510(k) Type
Traditional
Applicant
ELEKTA INSTRUMENT AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/1996
Days to Decision
90 days
Submission Type
Summary