BIODEX SYSTEM 3 MODEL S3S-AP AND MODEL S3D-3AP

K951770 · Biodex Medical Systems, Inc. · IKK · Nov 16, 1995 · Physical Medicine

Device Facts

Record IDK951770
Device NameBIODEX SYSTEM 3 MODEL S3S-AP AND MODEL S3D-3AP
ApplicantBiodex Medical Systems, Inc.
Product CodeIKK · Physical Medicine
Decision DateNov 16, 1995
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 890.1925
Device ClassClass 2
AttributesTherapeutic

Indications for Use

This device is designed for physical therapy to exercise, measure, evaluate and increase the strength of muscles and increase the Range of Motion (ROM) of joints.

Device Story

Isokinetic testing and evaluation system; used in physical therapy clinics; operated by clinicians. Device measures, evaluates, and exercises muscles; increases joint range of motion. System functions as digital isokinetic dynamometer; provides quantitative data on muscle strength and joint performance. Clinicians use output to guide rehabilitation protocols and monitor patient progress. Benefits include standardized assessment and controlled therapeutic exercise for musculoskeletal recovery.

Clinical Evidence

No clinical data provided. Safety and effectiveness confirmed via bench testing and comparison to legally marketed predicate devices.

Technological Characteristics

Class II Isokinetic Testing and Evaluation System (890.1925) and AC Powered Goniometer (888.1240). Digital design; utilizes components from previous Biodex systems. Software is a modification of existing cleared Biodex software. Operates as an AC-powered electromechanical system for musculoskeletal assessment.

Indications for Use

Indicated for patients requiring physical therapy for muscle strengthening and joint range of motion (ROM) improvement; used for exercise, measurement, and evaluation of muscle strength and joint function.

Regulatory Classification

Identification

An isokinetic testing and evaluation system is a rehabilitative exercise device intended for medical purposes, such as to measure, evaluate, and increase the strength of muscles and the range of motion of joints.

Special Controls

*Classification.* Class II (special controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to § 890.9.

Predicate Devices

Submission Summary (Full Text)

{0} EXHIBIT #14 NOV 16 1995 # SUMMARY OF SAFETY & EFFECTIVENESS # for BIODEX SYSTEM 3 K951770 This device is designed for physical therapy to exercise, measure, evaluate and increase the strength of muscles and increase the Range of Motion (ROM) of joints. This device is a CLASS II Isokinetic Testing and Evaluation System, Classification #890.1925 and an AC Powered Goniometer, Classification #888.1240. Biodex Medical Systems has determined that this device is substantially equivalent to medical devices currently in commerce, Biodex System 2 Auto Program cleared via K-91 5648 and Biodex Clinical Data Station cleared via K-913021 and the Cybex 6000 cleared via K-905525. NOV 1 1995 A determination of substantial equivalence is based upon: 1) The two cleared Biodex products combined are equivalent to the System 3 for their application and modes of operation. 2) The previous Biodex devices and System 3 use many of the same components. The software for the two devices are slight modifications of the same product. 3) The previous and new Biodex systems have the same fields of operation, except that one is an analog device and the other is a digital device. 4) The previous and new Biodex systems have the same safety requirements built into them. 5) The Cybex 6000 and Biodex System 3 are both digital designed products. The Cybex and Biodex are used for the same type of testing and rehabilitation. 6) This device is safe and effective for the application for which it is intended and has been tested to confirm its safety and effectiveness. Biodex Medical Systems continues to search appropriate sources for information relating to safety and effectiveness and maintains an in-house reporting system to identify adverse safety and effectiveness information. I hereby certify that this Summary of Safety and Effectiveness applies for the above indicated device. 4/12/95 Date CLYDE SCHLEIN CLYDE SCHLEIN, Director of Compliance Biodex Medical Systems, Inc. 20 Ramsay Road / P.O. Box 702 Shirley, New York 11967-0702 Phone: (516) 924-9000 Fax: (516) 924-8355 Registration #: 2431314
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