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PREVISION HIP SYSTEM WITH RECON RING

Page Type
Cleared 510(K)
510(k) Number
K102424
510(k) Type
Traditional
Applicant
AESCULAP IMPLANT SYSTEMS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2010
Days to Decision
106 days
Submission Type
Summary

PREVISION HIP SYSTEM WITH RECON RING

Page Type
Cleared 510(K)
510(k) Number
K102424
510(k) Type
Traditional
Applicant
AESCULAP IMPLANT SYSTEMS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2010
Days to Decision
106 days
Submission Type
Summary