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SUPERFIXATION(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K863343
510(k) Type
Traditional
Applicant
ORTHOPAEDIC DEVICE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/1986
Days to Decision
17 days

SUPERFIXATION(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K863343
510(k) Type
Traditional
Applicant
ORTHOPAEDIC DEVICE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/1986
Days to Decision
17 days