Last synced on 25 January 2026 at 3:41 am

VULCAN ABLATOR ELECTROSURGICAL PROBES, VULCAN LIGAMENT CHISEL ELECTROSURGICAL PROBES, MODEL 91000X,91002X,91300X

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003893
510(k) Type
Traditional
Applicant
Oratec Interventions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2001
Days to Decision
73 days
Submission Type
Summary

VULCAN ABLATOR ELECTROSURGICAL PROBES, VULCAN LIGAMENT CHISEL ELECTROSURGICAL PROBES, MODEL 91000X,91002X,91300X

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003893
510(k) Type
Traditional
Applicant
Oratec Interventions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2001
Days to Decision
73 days
Submission Type
Summary