Last synced on 30 May 2025 at 11:05 pm

M6-C Artificial Cervical Disc Instruments AS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220861
510(k) Type
Traditional
Applicant
Spinal Kinetics LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2022
Days to Decision
70 days
Submission Type
Summary

M6-C Artificial Cervical Disc Instruments AS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220861
510(k) Type
Traditional
Applicant
Spinal Kinetics LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2022
Days to Decision
70 days
Submission Type
Summary