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K3 BONE SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960533
510(k) Type
Traditional
Applicant
Kinetikos Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/25/1996
Days to Decision
47 days

K3 BONE SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960533
510(k) Type
Traditional
Applicant
Kinetikos Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/25/1996
Days to Decision
47 days