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SELBY II INSTRUMENTATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895296
510(k) Type
Traditional
Applicant
ADVANCED SPINE FIXATION
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/20/1990
Days to Decision
207 days

SELBY II INSTRUMENTATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895296
510(k) Type
Traditional
Applicant
ADVANCED SPINE FIXATION
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/20/1990
Days to Decision
207 days