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MODIFICATION TO LEKSELL SURGIPLAN WITH ATLASPACE

Page Type
Cleared 510(K)
510(k) Number
K013861
510(k) Type
Special
Applicant
ELEKTA INSTRUMENT AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/2001
Days to Decision
15 days
Submission Type
Summary

MODIFICATION TO LEKSELL SURGIPLAN WITH ATLASPACE

Page Type
Cleared 510(K)
510(k) Number
K013861
510(k) Type
Special
Applicant
ELEKTA INSTRUMENT AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/2001
Days to Decision
15 days
Submission Type
Summary