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ISOLA(TM) SPINE SYSTEM - ILIAC SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911528
510(k) Type
Traditional
Applicant
ACROMED CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
6/28/1991
Days to Decision
85 days

ISOLA(TM) SPINE SYSTEM - ILIAC SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911528
510(k) Type
Traditional
Applicant
ACROMED CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
6/28/1991
Days to Decision
85 days