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FDA 510(k)

MODEL 3031; CERVICAL SPINE SURFACE COIL

K-Number: K890666 · 1989-04-14

ApplicantMedical Advances, Inc.
Decision Date1989-04-14
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL 3031; CERVICAL SPINE SURFACE COIL 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 1989-04-14 under 510(k) number K890666. 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 MODEL 3031; CERVICAL SPINE SURFACE COIL?

MODEL 3031; CERVICAL SPINE SURFACE COIL is a medical device that received FDA 510(k) clearance on 1989-04-14. The listed applicant is Medical Advances, Inc.. The 510(k) number is K890666.

When did MODEL 3031; CERVICAL SPINE SURFACE COIL receive FDA 510(k) clearance?

MODEL 3031; CERVICAL SPINE SURFACE COIL received FDA 510(k) clearance on 1989-04-14, under 510(k) number K890666.

Who is the listed applicant for MODEL 3031; CERVICAL SPINE SURFACE COIL?

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 MODEL 3031; CERVICAL SPINE SURFACE COIL?

The FDA product code for MODEL 3031; CERVICAL SPINE SURFACE COIL is LNH.

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Other records listing Medical Advances, Inc. as applicant

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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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