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ELLIPSE LUMBAR POSTERIOR OSTEOSYNTHESIS SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K081165
510(k) Type
Traditional
Applicant
SPINEART
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
12/17/2008
Days to Decision
237 days
Submission Type
Summary

ELLIPSE LUMBAR POSTERIOR OSTEOSYNTHESIS SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K081165
510(k) Type
Traditional
Applicant
SPINEART
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
12/17/2008
Days to Decision
237 days
Submission Type
Summary