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ORTHOVITA PEEK SPACER

Page Type
Cleared 510(K)
510(k) Number
K101171
510(k) Type
Traditional
Applicant
ORTHOVITA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2011
Days to Decision
274 days
Submission Type
Summary

ORTHOVITA PEEK SPACER

Page Type
Cleared 510(K)
510(k) Number
K101171
510(k) Type
Traditional
Applicant
ORTHOVITA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2011
Days to Decision
274 days
Submission Type
Summary