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GO UNIVERSALK-WIRE FLUTED DRILL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954543
510(k) Type
Traditional
Applicant
GENESIS ORTHOPEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
12/8/1995
Days to Decision
71 days
Submission Type
Statement

GO UNIVERSALK-WIRE FLUTED DRILL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954543
510(k) Type
Traditional
Applicant
GENESIS ORTHOPEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
12/8/1995
Days to Decision
71 days
Submission Type
Statement