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KT2000 KNEE LIGAMENT ARTHROMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942059
510(k) Type
Traditional
Applicant
MEDMETRIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/20/1994
Days to Decision
144 days
Submission Type
Statement

KT2000 KNEE LIGAMENT ARTHROMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942059
510(k) Type
Traditional
Applicant
MEDMETRIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/20/1994
Days to Decision
144 days
Submission Type
Statement