Last synced on 20 December 2024 at 11:05 pm

VERTIS PNT CONTROL UNIT, MODEL CU 100; VERTIS PNT SAFEGUIDE-CERVICAL, MODEL SG 102-XXX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022241
510(k) Type
Traditional
Applicant
VERTIS NEUROSCIENCE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2002
Days to Decision
62 days
Submission Type
Summary

VERTIS PNT CONTROL UNIT, MODEL CU 100; VERTIS PNT SAFEGUIDE-CERVICAL, MODEL SG 102-XXX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022241
510(k) Type
Traditional
Applicant
VERTIS NEUROSCIENCE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2002
Days to Decision
62 days
Submission Type
Summary