FDA 510(k)

TRIGEN RETROGRADE FEMORAL, SUPRACONDYLAR AND TIBIAL NAILS

K-Number: K051557 · 2005-06-30

Decision Date2005-06-30

Product CodeJDS

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

TRIGEN RETROGRADE FEMORAL, SUPRACONDYLAR AND TIBIAL NAILS is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2005-06-30 under 510(k) number K051557. The device is classified under product code JDS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIGEN RETROGRADE FEMORAL, SUPRACONDYLAR AND TIBIAL NAILS?

TRIGEN RETROGRADE FEMORAL, SUPRACONDYLAR AND TIBIAL NAILS is a medical device that received FDA 510(k) clearance on 2005-06-30. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K051557.

When did TRIGEN RETROGRADE FEMORAL, SUPRACONDYLAR AND TIBIAL NAILS receive FDA 510(k) clearance?

TRIGEN RETROGRADE FEMORAL, SUPRACONDYLAR AND TIBIAL NAILS received FDA 510(k) clearance on 2005-06-30, under 510(k) number K051557.

Who is the listed applicant for TRIGEN RETROGRADE FEMORAL, SUPRACONDYLAR AND TIBIAL NAILS?

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

What is the FDA product code for TRIGEN RETROGRADE FEMORAL, SUPRACONDYLAR AND TIBIAL NAILS?

The FDA product code for TRIGEN RETROGRADE FEMORAL, SUPRACONDYLAR AND TIBIAL NAILS is JDS.

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Related Devices (Code: JDS)

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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.