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SENTRY POSTERIOR SPINAL SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K930710
510(k) Type
Traditional
Applicant
SOFAMOR DANEK MFG., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/1993
Days to Decision
232 days
Submission Type
Summary

SENTRY POSTERIOR SPINAL SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K930710
510(k) Type
Traditional
Applicant
SOFAMOR DANEK MFG., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/1993
Days to Decision
232 days
Submission Type
Summary