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FDA 510(k)

SPINAL MARKER

K-Number: K944188 · 1995-04-13

ApplicantLeibinger L.P.
Decision Date1995-04-13
Product CodeLXH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SPINAL MARKER is the device name listed in this FDA 510(k) record. The listed applicant is Leibinger L.P.. It received FDA 510(k) clearance on 1995-04-13 under 510(k) number K944188. The device is classified under product code LXH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPINAL MARKER?

SPINAL MARKER is a medical device that received FDA 510(k) clearance on 1995-04-13. The listed applicant is Leibinger L.P.. The 510(k) number is K944188.

When did SPINAL MARKER receive FDA 510(k) clearance?

SPINAL MARKER received FDA 510(k) clearance on 1995-04-13, under 510(k) number K944188.

Who is the listed applicant for SPINAL MARKER?

The FDA 510(k) record lists Leibinger L.P. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPINAL MARKER?

The FDA product code for SPINAL MARKER is LXH.

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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.

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