Last synced on 25 April 2025 at 11:05 pm

DIVERGENCE-L ANTERIOR/OBLIQUE LUMBAR FUSION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162212
510(k) Type
Traditional
Applicant
MEDTRONIC SOFAMOR DANEK USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/2017
Days to Decision
284 days
Submission Type
Summary

DIVERGENCE-L ANTERIOR/OBLIQUE LUMBAR FUSION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162212
510(k) Type
Traditional
Applicant
MEDTRONIC SOFAMOR DANEK USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/2017
Days to Decision
284 days
Submission Type
Summary