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FDA 510(k)

THORACIC/LUMBAR SPINE 8 RACETRACK COIL, 3080-64

K-Number: K901241 · 1990-04-25

ApplicantMedical Advances, Inc.
Decision Date1990-04-25
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

THORACIC/LUMBAR SPINE 8 RACETRACK COIL, 3080-64 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Advances, Inc.. It received FDA 510(k) clearance on 1990-04-25 under 510(k) number K901241. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THORACIC/LUMBAR SPINE 8 RACETRACK COIL, 3080-64?

THORACIC/LUMBAR SPINE 8 RACETRACK COIL, 3080-64 is a medical device that received FDA 510(k) clearance on 1990-04-25. The listed applicant is Medical Advances, Inc.. The 510(k) number is K901241.

When did THORACIC/LUMBAR SPINE 8 RACETRACK COIL, 3080-64 receive FDA 510(k) clearance?

THORACIC/LUMBAR SPINE 8 RACETRACK COIL, 3080-64 received FDA 510(k) clearance on 1990-04-25, under 510(k) number K901241.

Who is the listed applicant for THORACIC/LUMBAR SPINE 8 RACETRACK COIL, 3080-64?

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

What is the FDA product code for THORACIC/LUMBAR SPINE 8 RACETRACK COIL, 3080-64?

The FDA product code for THORACIC/LUMBAR SPINE 8 RACETRACK COIL, 3080-64 is LNH.

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Other records listing Medical Advances, Inc. as applicant

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Related Devices (Code: LNH)

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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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