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NEOSS PROACTIVE IMPLANT

Page Type
Cleared 510(K)
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)
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