Last synced on 30 May 2025 at 11:05 pm

prodisc C SK, prodisc C Nova, and prodisc C Vivo Instruments

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221848
510(k) Type
Traditional
Applicant
Centinel Spine LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2022
Days to Decision
56 days
Submission Type
Summary

prodisc C SK, prodisc C Nova, and prodisc C Vivo Instruments

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221848
510(k) Type
Traditional
Applicant
Centinel Spine LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2022
Days to Decision
56 days
Submission Type
Summary