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SAGITTAL & ROTARY ACT/PASS KNEE LIGAMENT TESTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861622
510(k) Type
Traditional
Applicant
ORTHOPEDIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/1986
Days to Decision
28 days

SAGITTAL & ROTARY ACT/PASS KNEE LIGAMENT TESTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861622
510(k) Type
Traditional
Applicant
ORTHOPEDIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/1986
Days to Decision
28 days