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ADI 9000/9001 ARTHROSCOPE AND ACCESSORIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992621
510(k) Type
Traditional
Applicant
ADVANCED DIAGNOSTICS & INTERVENTIONS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/1999
Days to Decision
95 days
Submission Type
Statement

ADI 9000/9001 ARTHROSCOPE AND ACCESSORIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992621
510(k) Type
Traditional
Applicant
ADVANCED DIAGNOSTICS & INTERVENTIONS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/1999
Days to Decision
95 days
Submission Type
Statement