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ZENITH PLATE SYSTEM, ANTERIOR SPINAL INSTRUMENTATION

Page Type
Cleared 510(K)
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)
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