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FDA 510(k)

ARTSCAN CARTILAGE STIFFNESS TESTING DEVICE

K-Number: K010303 · 2001-09-11

ApplicantArtscan Medical Innovations
Decision Date2001-09-11
Product CodeNGR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTSCAN CARTILAGE STIFFNESS TESTING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Artscan Medical Innovations. It received FDA 510(k) clearance on 2001-09-11 under 510(k) number K010303. The device is classified under product code NGR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTSCAN CARTILAGE STIFFNESS TESTING DEVICE?

ARTSCAN CARTILAGE STIFFNESS TESTING DEVICE is a medical device that received FDA 510(k) clearance on 2001-09-11. The listed applicant is Artscan Medical Innovations. The 510(k) number is K010303.

When did ARTSCAN CARTILAGE STIFFNESS TESTING DEVICE receive FDA 510(k) clearance?

ARTSCAN CARTILAGE STIFFNESS TESTING DEVICE received FDA 510(k) clearance on 2001-09-11, under 510(k) number K010303.

Who is the listed applicant for ARTSCAN CARTILAGE STIFFNESS TESTING DEVICE?

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

What is the FDA product code for ARTSCAN CARTILAGE STIFFNESS TESTING DEVICE?

The FDA product code for ARTSCAN CARTILAGE STIFFNESS TESTING DEVICE is NGR.

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Related Devices (Code: NGR)

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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