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FDA 510(k)

ORTHO-PLEX-REHABILITATION SYSTEM

K-Number: K920686 · 1992-06-11

ApplicantPlexus Intl., Inc.
Decision Date1992-06-11
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ORTHO-PLEX-REHABILITATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Plexus Intl., Inc.. It received FDA 510(k) clearance on 1992-06-11 under 510(k) number K920686. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHO-PLEX-REHABILITATION SYSTEM?

ORTHO-PLEX-REHABILITATION SYSTEM is a medical device that received FDA 510(k) clearance on 1992-06-11. The listed applicant is Plexus Intl., Inc.. The 510(k) number is K920686.

When did ORTHO-PLEX-REHABILITATION SYSTEM receive FDA 510(k) clearance?

ORTHO-PLEX-REHABILITATION SYSTEM received FDA 510(k) clearance on 1992-06-11, under 510(k) number K920686.

Who is the listed applicant for ORTHO-PLEX-REHABILITATION SYSTEM?

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

What is the FDA product code for ORTHO-PLEX-REHABILITATION SYSTEM?

The FDA product code for ORTHO-PLEX-REHABILITATION SYSTEM is BXB.

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Related Devices (Code: BXB)

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.

K072887G-TRAINER MEDICALAlter-G, Inc.K003272FLO-BOOTDiscovery Group, LLCK952975ANKLE CALF EXERCISER PHLEBOPUMPPrevent Products, Inc.K953456E-Z FLEXFluid Motion Biotechnologies, Inc.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.

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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