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ELLIPSE LUMBAR POSTERIOR OSTEOSYNTHESIS SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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