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FDA 510(k)

FLEXIBLE PHASED ARRAY SPINE COIL

K-Number: K960497 · 1996-07-05

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1996-07-05
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FLEXIBLE PHASED ARRAY SPINE COIL is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems (Cleveland), Inc.. It received FDA 510(k) clearance on 1996-07-05 under 510(k) number K960497. 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 FLEXIBLE PHASED ARRAY SPINE COIL?

FLEXIBLE PHASED ARRAY SPINE COIL is a medical device that received FDA 510(k) clearance on 1996-07-05. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K960497.

When did FLEXIBLE PHASED ARRAY SPINE COIL receive FDA 510(k) clearance?

FLEXIBLE PHASED ARRAY SPINE COIL received FDA 510(k) clearance on 1996-07-05, under 510(k) number K960497.

Who is the listed applicant for FLEXIBLE PHASED ARRAY SPINE COIL?

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

What is the FDA product code for FLEXIBLE PHASED ARRAY SPINE COIL?

The FDA product code for FLEXIBLE PHASED ARRAY SPINE COIL is 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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