FDA 510(k)

PHASED ARRAY CERVICAL SPINE COIL, MODEL #125GE-64

K-Number: K983222 · 1998-10-08

Decision Date1998-10-08

Product CodeMOS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

PHASED ARRAY CERVICAL SPINE COIL, MODEL #125GE-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 1998-10-08 under 510(k) number K983222. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHASED ARRAY CERVICAL SPINE COIL, MODEL #125GE-64?

PHASED ARRAY CERVICAL SPINE COIL, MODEL #125GE-64 is a medical device that received FDA 510(k) clearance on 1998-10-08. The listed applicant is Medical Advances, Inc.. The 510(k) number is K983222.

When did PHASED ARRAY CERVICAL SPINE COIL, MODEL #125GE-64 receive FDA 510(k) clearance?

PHASED ARRAY CERVICAL SPINE COIL, MODEL #125GE-64 received FDA 510(k) clearance on 1998-10-08, under 510(k) number K983222.

Who is the listed applicant for PHASED ARRAY CERVICAL SPINE COIL, MODEL #125GE-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 PHASED ARRAY CERVICAL SPINE COIL, MODEL #125GE-64?

The FDA product code for PHASED ARRAY CERVICAL SPINE COIL, MODEL #125GE-64 is MOS.

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Other records listing Medical Advances, Inc. as applicant

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Related Devices (Code: MOS)

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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.