Last synced on 25 April 2025 at 11:05 pm

Blustone Synergy Lumbar Interbody Fusion System (Basalt, Magma, Obsidian), Blustone Synergy Cervical Interbody Fusion System (Slate)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171893
510(k) Type
Traditional
Applicant
Bluestone Synergy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/2017
Days to Decision
74 days
Submission Type
Summary

Blustone Synergy Lumbar Interbody Fusion System (Basalt, Magma, Obsidian), Blustone Synergy Cervical Interbody Fusion System (Slate)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171893
510(k) Type
Traditional
Applicant
Bluestone Synergy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/2017
Days to Decision
74 days
Submission Type
Summary