Last synced on 14 November 2025 at 11:06 pm

K2 BONE SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K960537
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

K2 BONE SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K960537
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