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NEOSS PROACTIVE IMPLANT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083561
510(k) Type
Special
Applicant
Neoss, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/2009
Days to Decision
71 days
Submission Type
Summary

NEOSS PROACTIVE IMPLANT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083561
510(k) Type
Special
Applicant
Neoss, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/2009
Days to Decision
71 days
Submission Type
Summary