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INDUS ANTERIOR CERVICAL PLATE SYSTEM, MODEL IM3XXX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073232
510(k) Type
Traditional
Applicant
Spinefrontier, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/2008
Days to Decision
97 days
Submission Type
Summary

INDUS ANTERIOR CERVICAL PLATE SYSTEM, MODEL IM3XXX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073232
510(k) Type
Traditional
Applicant
Spinefrontier, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/2008
Days to Decision
97 days
Submission Type
Summary