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N8TIVE ACL ANATOMIC RECONSTRUCTION SYSTEM, N8TIVE ACL FEMORAL IMPLANT, N8TIVE ACL TIBIAL IMPLANT, VARIOUS CLASS I ANCILL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133606
510(k) Type
Traditional
Applicant
ARTHROCARE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/2014
Days to Decision
127 days
Submission Type
Summary

N8TIVE ACL ANATOMIC RECONSTRUCTION SYSTEM, N8TIVE ACL FEMORAL IMPLANT, N8TIVE ACL TIBIAL IMPLANT, VARIOUS CLASS I ANCILL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133606
510(k) Type
Traditional
Applicant
ARTHROCARE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/2014
Days to Decision
127 days
Submission Type
Summary