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FDA 510(k)

SPINALSCOPICS

K-Number: K970862 · 1997-04-08

ApplicantQuantimetrix Corp.
Decision Date1997-04-08
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SPINALSCOPICS is the device name listed in this FDA 510(k) record. The listed applicant is Quantimetrix Corp.. It received FDA 510(k) clearance on 1997-04-08 under 510(k) number K970862. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPINALSCOPICS?

SPINALSCOPICS is a medical device that received FDA 510(k) clearance on 1997-04-08. The listed applicant is Quantimetrix Corp.. The 510(k) number is K970862.

When did SPINALSCOPICS receive FDA 510(k) clearance?

SPINALSCOPICS received FDA 510(k) clearance on 1997-04-08, under 510(k) number K970862.

Who is the listed applicant for SPINALSCOPICS?

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

What is the FDA product code for SPINALSCOPICS?

The FDA product code for SPINALSCOPICS is JJY.

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Other records listing Quantimetrix Corp. as applicant

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Related Devices (Code: JJY)

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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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