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STORZ PREMIERE II MICROSURGICAL SYSTEM (CX SERIES)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961310
510(k) Type
Traditional
Applicant
STORZ INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1996
Days to Decision
84 days
Submission Type
Summary

STORZ PREMIERE II MICROSURGICAL SYSTEM (CX SERIES)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961310
510(k) Type
Traditional
Applicant
STORZ INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1996
Days to Decision
84 days
Submission Type
Summary