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FDA 510(k)

MODIFICATION TO: TITANIUM TELEGRAPH HUMERAL NAIL

K-Number: K052058 · 2005-08-22

ApplicantFournitures Hospitalieres Industrie
Decision Date2005-08-22
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO: TITANIUM TELEGRAPH HUMERAL NAIL is the device name listed in this FDA 510(k) record. The listed applicant is Fournitures Hospitalieres Industrie. It received FDA 510(k) clearance on 2005-08-22 under 510(k) number K052058. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO: TITANIUM TELEGRAPH HUMERAL NAIL?

MODIFICATION TO: TITANIUM TELEGRAPH HUMERAL NAIL is a medical device that received FDA 510(k) clearance on 2005-08-22. The listed applicant is Fournitures Hospitalieres Industrie. The 510(k) number is K052058.

When did MODIFICATION TO: TITANIUM TELEGRAPH HUMERAL NAIL receive FDA 510(k) clearance?

MODIFICATION TO: TITANIUM TELEGRAPH HUMERAL NAIL received FDA 510(k) clearance on 2005-08-22, under 510(k) number K052058.

Who is the listed applicant for MODIFICATION TO: TITANIUM TELEGRAPH HUMERAL NAIL?

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

What is the FDA product code for MODIFICATION TO: TITANIUM TELEGRAPH HUMERAL NAIL?

The FDA product code for MODIFICATION TO: TITANIUM TELEGRAPH HUMERAL NAIL is HSB.

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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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