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FDA 510(k)

SORBIE TOTAL ELBOW SYSTEM

K-Number: K955099 · 1996-02-05

ApplicantWrightmedicaltechnologyinc
Decision Date1996-02-05
Product CodeJDB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SORBIE TOTAL ELBOW SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 1996-02-05 under 510(k) number K955099. The device is classified under product code JDB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SORBIE TOTAL ELBOW SYSTEM?

SORBIE TOTAL ELBOW SYSTEM is a medical device that received FDA 510(k) clearance on 1996-02-05. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K955099.

When did SORBIE TOTAL ELBOW SYSTEM receive FDA 510(k) clearance?

SORBIE TOTAL ELBOW SYSTEM received FDA 510(k) clearance on 1996-02-05, under 510(k) number K955099.

Who is the listed applicant for SORBIE TOTAL ELBOW SYSTEM?

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

What is the FDA product code for SORBIE TOTAL ELBOW SYSTEM?

The FDA product code for SORBIE TOTAL ELBOW SYSTEM is JDB.

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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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