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FDA 510(k)

BARNES FEMORAL LENGTHENING DEVICE

K-Number: K895243 · 1990-08-10

ApplicantPiedmont Sports Medicine & Orthopaedic Clinic
Decision Date1990-08-10
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BARNES FEMORAL LENGTHENING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Piedmont Sports Medicine & Orthopaedic Clinic. It received FDA 510(k) clearance on 1990-08-10 under 510(k) number K895243. 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 BARNES FEMORAL LENGTHENING DEVICE?

BARNES FEMORAL LENGTHENING DEVICE is a medical device that received FDA 510(k) clearance on 1990-08-10. The listed applicant is Piedmont Sports Medicine & Orthopaedic Clinic. The 510(k) number is K895243.

When did BARNES FEMORAL LENGTHENING DEVICE receive FDA 510(k) clearance?

BARNES FEMORAL LENGTHENING DEVICE received FDA 510(k) clearance on 1990-08-10, under 510(k) number K895243.

Who is the listed applicant for BARNES FEMORAL LENGTHENING DEVICE?

The FDA 510(k) record lists Piedmont Sports Medicine & Orthopaedic Clinic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BARNES FEMORAL LENGTHENING DEVICE?

The FDA product code for BARNES FEMORAL LENGTHENING DEVICE is HRS.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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