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FEMORAL CEMENT REMOVAL INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K840735
510(k) Type
Traditional
Applicant
AMTECH SCIENTIFIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/1984
Days to Decision
83 days

FEMORAL CEMENT REMOVAL INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K840735
510(k) Type
Traditional
Applicant
AMTECH SCIENTIFIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/1984
Days to Decision
83 days