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FDA 510(k)

LAMOREUX-OSI ELECTROGONIOMETER

K-Number: K831040 · 1983-07-12

ApplicantOrthopedic Systems, Inc.
Decision Date1983-07-12
Product CodeKQX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LAMOREUX-OSI ELECTROGONIOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Systems, Inc.. It received FDA 510(k) clearance on 1983-07-12 under 510(k) number K831040. The device is classified under product code KQX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAMOREUX-OSI ELECTROGONIOMETER?

LAMOREUX-OSI ELECTROGONIOMETER is a medical device that received FDA 510(k) clearance on 1983-07-12. The listed applicant is Orthopedic Systems, Inc.. The 510(k) number is K831040.

When did LAMOREUX-OSI ELECTROGONIOMETER receive FDA 510(k) clearance?

LAMOREUX-OSI ELECTROGONIOMETER received FDA 510(k) clearance on 1983-07-12, under 510(k) number K831040.

Who is the listed applicant for LAMOREUX-OSI ELECTROGONIOMETER?

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

What is the FDA product code for LAMOREUX-OSI ELECTROGONIOMETER?

The FDA product code for LAMOREUX-OSI ELECTROGONIOMETER is KQX.

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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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Other records listing Orthopedic Systems, Inc. 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.

K952495ANCHORS AWAY SOFT TISSUE ATTACHMENT SYSTEMK920256SPINE MOTION ANALYZER WITH EMGK910736JACKSON MULTIPURPOSE OPERATING TABLEK910031PARK CITY SHOULDER POSITIONERK903938C FIT CUPK892503NUFFIELD TOTAL KNEE

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Related Devices (Code: KQX)

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.

K011827ORTELIUS 800Orthoscan , Ltd.K971079INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWAREInterlogics, Inc.K9623773D-SPINESkill Technologies, Inc.K961212SPINAL TOUCHFasstechK954647INCLINOMETERJ-Tech, Inc.K943929DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS)Greenleaf Medical Systems, Inc.

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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