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CONMED LINVATEC INTERCEPT IMPLANT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092998
510(k) Type
Traditional
Applicant
Linvatec Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2009
Days to Decision
86 days
Submission Type
Summary

CONMED LINVATEC INTERCEPT IMPLANT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092998
510(k) Type
Traditional
Applicant
Linvatec Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2009
Days to Decision
86 days
Submission Type
Summary