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MODIFICATION TO LEKSELL STEREOTACTIC SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K031980
510(k) Type
Special
Applicant
ELEKTA INSTRUMENT AB
Country
Sweden
FDA Decision
Substantially Equivalent
Decision Date
7/25/2003
Days to Decision
29 days
Submission Type
Statement

MODIFICATION TO LEKSELL STEREOTACTIC SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K031980
510(k) Type
Special
Applicant
ELEKTA INSTRUMENT AB
Country
Sweden
FDA Decision
Substantially Equivalent
Decision Date
7/25/2003
Days to Decision
29 days
Submission Type
Statement