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FDA 510(k)

CHARLOTTE SMALL MTP FUSION PLATE

K-Number: K051884 · 2005-08-05

Decision Date2005-08-05
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CHARLOTTE SMALL MTP FUSION PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2005-08-05 under 510(k) number K051884. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHARLOTTE SMALL MTP FUSION PLATE?

CHARLOTTE SMALL MTP FUSION PLATE is a medical device that received FDA 510(k) clearance on 2005-08-05. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K051884.

When did CHARLOTTE SMALL MTP FUSION PLATE receive FDA 510(k) clearance?

CHARLOTTE SMALL MTP FUSION PLATE received FDA 510(k) clearance on 2005-08-05, under 510(k) number K051884.

Who is the listed applicant for CHARLOTTE SMALL MTP FUSION PLATE?

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 CHARLOTTE SMALL MTP FUSION PLATE?

The FDA product code for CHARLOTTE SMALL MTP FUSION PLATE is HRS.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Wrightmedicaltechnologyinc as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 268 devices →

Related Devices (Code: HRS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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