Last synced on 9 May 2025 at 11:05 pm

SPACEVISION CAGE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042930
510(k) Type
Traditional
Applicant
SPINEVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/28/2004
Days to Decision
67 days
Submission Type
Summary

SPACEVISION CAGE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042930
510(k) Type
Traditional
Applicant
SPINEVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/28/2004
Days to Decision
67 days
Submission Type
Summary