FDA 510(k)

DEFLECTABLE TAC ELECTROTHERMAL PROBE

K-Number: K990859 · 1999-06-14

Decision Date1999-06-14

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

DEFLECTABLE TAC ELECTROTHERMAL PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Oratec Interventions, Inc.. It received FDA 510(k) clearance on 1999-06-14 under 510(k) number K990859. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEFLECTABLE TAC ELECTROTHERMAL PROBE?

DEFLECTABLE TAC ELECTROTHERMAL PROBE is a medical device that received FDA 510(k) clearance on 1999-06-14. The listed applicant is Oratec Interventions, Inc.. The 510(k) number is K990859.

When did DEFLECTABLE TAC ELECTROTHERMAL PROBE receive FDA 510(k) clearance?

DEFLECTABLE TAC ELECTROTHERMAL PROBE received FDA 510(k) clearance on 1999-06-14, under 510(k) number K990859.

Who is the listed applicant for DEFLECTABLE TAC ELECTROTHERMAL PROBE?

The FDA 510(k) record lists Oratec Interventions, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEFLECTABLE TAC ELECTROTHERMAL PROBE?

The FDA product code for DEFLECTABLE TAC ELECTROTHERMAL PROBE is GEI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.