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DRILL MODULES MODELS 2116/2117

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914346
510(k) Type
Traditional
Applicant
MICRO SURGICAL INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/1991
Days to Decision
61 days
Submission Type
Statement

DRILL MODULES MODELS 2116/2117

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914346
510(k) Type
Traditional
Applicant
MICRO SURGICAL INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/1991
Days to Decision
61 days
Submission Type
Statement