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IdentiTi and Transcend Interbody Systems: IndentiTi Cervical Porous Ti Interbody System, IdentiTi NanoTec Cervical Interbody System, Transcend Cervical PEEK Interbody System, Transcend NanoTec Cervical Interbody System, IdentiTi Cervical Standalone Interbody System, IdentiTi NanoTec Cervical Standalone Interbody Sytem

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222973
510(k) Type
Traditional
Applicant
Alphatec Spine Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2022
Days to Decision
50 days
Submission Type
Summary

IdentiTi and Transcend Interbody Systems: IndentiTi Cervical Porous Ti Interbody System, IdentiTi NanoTec Cervical Interbody System, Transcend Cervical PEEK Interbody System, Transcend NanoTec Cervical Interbody System, IdentiTi Cervical Standalone Interbody System, IdentiTi NanoTec Cervical Standalone Interbody Sytem

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222973
510(k) Type
Traditional
Applicant
Alphatec Spine Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2022
Days to Decision
50 days
Submission Type
Summary