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FDA 510(k)

TROKABONE, TROKABONE STERNAL

K-Number: K070179 · 2007-03-07

ApplicantPAJUNK GmbH Medizintechnologie
Decision Date2007-03-07
Product CodeFCG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TROKABONE, TROKABONE STERNAL is the device name listed in this FDA 510(k) record. The listed applicant is PAJUNK GmbH Medizintechnologie. It received FDA 510(k) clearance on 2007-03-07 under 510(k) number K070179. The device is classified under product code FCG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TROKABONE, TROKABONE STERNAL?

TROKABONE, TROKABONE STERNAL is a medical device that received FDA 510(k) clearance on 2007-03-07. The listed applicant is PAJUNK GmbH Medizintechnologie. The 510(k) number is K070179.

When did TROKABONE, TROKABONE STERNAL receive FDA 510(k) clearance?

TROKABONE, TROKABONE STERNAL received FDA 510(k) clearance on 2007-03-07, under 510(k) number K070179.

Who is the listed applicant for TROKABONE, TROKABONE STERNAL?

The FDA 510(k) record lists PAJUNK GmbH Medizintechnologie as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TROKABONE, TROKABONE STERNAL?

The FDA product code for TROKABONE, TROKABONE STERNAL is FCG.

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Official Source

View on FDA Database →

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

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