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MODIFICATION TO LEKSELL STEREOTACTIC SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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