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IdentiTi Porous Ti Interbody System, Transcend PEEK Interbody System, IdentiTi NanoTec Interbody System, Transcend NanoTec Interbody System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211805
510(k) Type
Traditional
Applicant
Alphatec Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/2021
Days to Decision
103 days
Submission Type
Summary

IdentiTi Porous Ti Interbody System, Transcend PEEK Interbody System, IdentiTi NanoTec Interbody System, Transcend NanoTec Interbody System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211805
510(k) Type
Traditional
Applicant
Alphatec Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/2021
Days to Decision
103 days
Submission Type
Summary