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FDA 510(k)

FEMORAL HEADS, 2.5 AND 7.5 MM NECK LENGTH

K-Number: K122504 · 2012-10-10

Decision Date2012-10-10
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FEMORAL HEADS, 2.5 AND 7.5 MM NECK LENGTH is the device name listed in this FDA 510(k) record. The listed applicant is United Orthopedic Corporation. It received FDA 510(k) clearance on 2012-10-10 under 510(k) number K122504. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FEMORAL HEADS, 2.5 AND 7.5 MM NECK LENGTH?

FEMORAL HEADS, 2.5 AND 7.5 MM NECK LENGTH is a medical device that received FDA 510(k) clearance on 2012-10-10. The listed applicant is United Orthopedic Corporation. The 510(k) number is K122504.

When did FEMORAL HEADS, 2.5 AND 7.5 MM NECK LENGTH receive FDA 510(k) clearance?

FEMORAL HEADS, 2.5 AND 7.5 MM NECK LENGTH received FDA 510(k) clearance on 2012-10-10, under 510(k) number K122504.

Who is the listed applicant for FEMORAL HEADS, 2.5 AND 7.5 MM NECK LENGTH?

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

What is the FDA product code for FEMORAL HEADS, 2.5 AND 7.5 MM NECK LENGTH?

The FDA product code for FEMORAL HEADS, 2.5 AND 7.5 MM NECK LENGTH is LPH.

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 United Orthopedic Corporation 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.

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Related Devices (Code: LPH)

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

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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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