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FDA 510(k)

HOFFMAN LEG LENGTHENING DEVICE

K-Number: K802776 · 1980-11-19

ApplicantHowmedica Corp.
Decision Date1980-11-19
Product CodeJEC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HOFFMAN LEG LENGTHENING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1980-11-19 under 510(k) number K802776. The device is classified under product code JEC. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOFFMAN LEG LENGTHENING DEVICE?

HOFFMAN LEG LENGTHENING DEVICE is a medical device that received FDA 510(k) clearance on 1980-11-19. The listed applicant is Howmedica Corp.. The 510(k) number is K802776.

When did HOFFMAN LEG LENGTHENING DEVICE receive FDA 510(k) clearance?

HOFFMAN LEG LENGTHENING DEVICE received FDA 510(k) clearance on 1980-11-19, under 510(k) number K802776.

Who is the listed applicant for HOFFMAN LEG LENGTHENING DEVICE?

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

What is the FDA product code for HOFFMAN LEG LENGTHENING DEVICE?

The FDA product code for HOFFMAN LEG LENGTHENING DEVICE is JEC.

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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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