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FDA 510(k)

MODUS TRILOCK 2.0/2.3/2.5

K-Number: K071612 · 2007-09-11

ApplicantMedartis AG
Decision Date2007-09-11
Product CodeJEY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MODUS TRILOCK 2.0/2.3/2.5 is the device name listed in this FDA 510(k) record. The listed applicant is Medartis AG. It received FDA 510(k) clearance on 2007-09-11 under 510(k) number K071612. The device is classified under product code JEY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODUS TRILOCK 2.0/2.3/2.5?

MODUS TRILOCK 2.0/2.3/2.5 is a medical device that received FDA 510(k) clearance on 2007-09-11. The listed applicant is Medartis AG. The 510(k) number is K071612.

When did MODUS TRILOCK 2.0/2.3/2.5 receive FDA 510(k) clearance?

MODUS TRILOCK 2.0/2.3/2.5 received FDA 510(k) clearance on 2007-09-11, under 510(k) number K071612.

Who is the listed applicant for MODUS TRILOCK 2.0/2.3/2.5?

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

What is the FDA product code for MODUS TRILOCK 2.0/2.3/2.5?

The FDA product code for MODUS TRILOCK 2.0/2.3/2.5 is JEY.

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Related Devices (Code: JEY)

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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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