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FDA 510(k)

LP ARTHROSCOPIC THIGH HOLDING DEVICE

K-Number: K864513 · 1986-11-25

ApplicantTwin Falls Orthopedic Associates, P.A.
Decision Date1986-11-25
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LP ARTHROSCOPIC THIGH HOLDING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Twin Falls Orthopedic Associates, P.A.. It received FDA 510(k) clearance on 1986-11-25 under 510(k) number K864513. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LP ARTHROSCOPIC THIGH HOLDING DEVICE?

LP ARTHROSCOPIC THIGH HOLDING DEVICE is a medical device that received FDA 510(k) clearance on 1986-11-25. The listed applicant is Twin Falls Orthopedic Associates, P.A.. The 510(k) number is K864513.

When did LP ARTHROSCOPIC THIGH HOLDING DEVICE receive FDA 510(k) clearance?

LP ARTHROSCOPIC THIGH HOLDING DEVICE received FDA 510(k) clearance on 1986-11-25, under 510(k) number K864513.

Who is the listed applicant for LP ARTHROSCOPIC THIGH HOLDING DEVICE?

The FDA 510(k) record lists Twin Falls Orthopedic Associates, P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LP ARTHROSCOPIC THIGH HOLDING DEVICE?

The FDA product code for LP ARTHROSCOPIC THIGH HOLDING DEVICE is HRX.

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Related Devices (Code: HRX)

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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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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