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FDA 510(k)

SPINOSCOPE

K-Number: K872836 · 1987-09-29

ApplicantDiagnospine Fabrication, Inc.
Decision Date1987-09-29
Product CodeIKN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SPINOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Diagnospine Fabrication, Inc.. It received FDA 510(k) clearance on 1987-09-29 under 510(k) number K872836. The device is classified under product code IKN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPINOSCOPE?

SPINOSCOPE is a medical device that received FDA 510(k) clearance on 1987-09-29. The listed applicant is Diagnospine Fabrication, Inc.. The 510(k) number is K872836.

When did SPINOSCOPE receive FDA 510(k) clearance?

SPINOSCOPE received FDA 510(k) clearance on 1987-09-29, under 510(k) number K872836.

Who is the listed applicant for SPINOSCOPE?

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

What is the FDA product code for SPINOSCOPE?

The FDA product code for SPINOSCOPE is IKN.

Related Clinical Trials

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Related Devices (Code: IKN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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