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CARBIDE CUTTING INSTRUMENT/INTRAARTICU

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802598
510(k) Type
Traditional
Applicant
THE ANSPACH EFFORT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/1980
Days to Decision
29 days

CARBIDE CUTTING INSTRUMENT/INTRAARTICU

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802598
510(k) Type
Traditional
Applicant
THE ANSPACH EFFORT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/1980
Days to Decision
29 days