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FLEXIBLE REAMER, GUIDE WIRE SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790307
510(k) Type
Traditional
Applicant
3M COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/1979
Days to Decision
9 days

FLEXIBLE REAMER, GUIDE WIRE SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790307
510(k) Type
Traditional
Applicant
3M COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/1979
Days to Decision
9 days