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ENSPLINT TM BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K080778
510(k) Type
Traditional
Applicant
SONOMA ORTHOPEDIC PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/2008
Days to Decision
113 days
Submission Type
Summary

ENSPLINT TM BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K080778
510(k) Type
Traditional
Applicant
SONOMA ORTHOPEDIC PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/2008
Days to Decision
113 days
Submission Type
Summary