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FDA 510(k)

ARTROMOT MULTI DIRECTIONAL ANKLE CPM

K-Number: K924484 · 1993-03-22

ApplicantBuckman Co., Inc.
Decision Date1993-03-22
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ARTROMOT MULTI DIRECTIONAL ANKLE CPM is the device name listed in this FDA 510(k) record. The listed applicant is Buckman Co., Inc.. It received FDA 510(k) clearance on 1993-03-22 under 510(k) number K924484. 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 ARTROMOT MULTI DIRECTIONAL ANKLE CPM?

ARTROMOT MULTI DIRECTIONAL ANKLE CPM is a medical device that received FDA 510(k) clearance on 1993-03-22. The listed applicant is Buckman Co., Inc.. The 510(k) number is K924484.

When did ARTROMOT MULTI DIRECTIONAL ANKLE CPM receive FDA 510(k) clearance?

ARTROMOT MULTI DIRECTIONAL ANKLE CPM received FDA 510(k) clearance on 1993-03-22, under 510(k) number K924484.

Who is the listed applicant for ARTROMOT MULTI DIRECTIONAL ANKLE CPM?

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

What is the FDA product code for ARTROMOT MULTI DIRECTIONAL ANKLE CPM?

The FDA product code for ARTROMOT MULTI DIRECTIONAL ANKLE CPM is BXB.

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Other records listing Buckman Co., Inc. as applicant

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K961320CROSS MEDICAL BONE PLATE SYSTEM/ CM BONE PLATE SYSTEM/CROSS TI BONE PLATE SYSTEMK974641FUTURELASE 3000/3002 ERBIUM LASER SYSTEMK964252ORTHOCHUCKK950099SYNERGY(TM) TI POSTERIOR SPINAL SYSTEMK960451WEBB-MORLEY SPINE SYSTEMK950999KSF POSTERIOR SPINGAL FIXATOR FOR SEVERE SPONDYLOLISTHESIS

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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.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.

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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