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ZENITH PLATE SYSTEM, ANTERIOR SPINAL INSTRUMENTATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001535
510(k) Type
Traditional
Applicant
ORTHOTEC, L.L.C.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/2001
Days to Decision
307 days
Submission Type
Summary

ZENITH PLATE SYSTEM, ANTERIOR SPINAL INSTRUMENTATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001535
510(k) Type
Traditional
Applicant
ORTHOTEC, L.L.C.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/2001
Days to Decision
307 days
Submission Type
Summary