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FDA 510(k)

VIDAR BONE TRACK SYSTEM SOFTWARE

K-Number: K024171 · 2003-03-04

ApplicantVidar Systems Corp.
Decision Date2003-03-04
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VIDAR BONE TRACK SYSTEM SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Vidar Systems Corp.. It received FDA 510(k) clearance on 2003-03-04 under 510(k) number K024171. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIDAR BONE TRACK SYSTEM SOFTWARE?

VIDAR BONE TRACK SYSTEM SOFTWARE is a medical device that received FDA 510(k) clearance on 2003-03-04. The listed applicant is Vidar Systems Corp.. The 510(k) number is K024171.

When did VIDAR BONE TRACK SYSTEM SOFTWARE receive FDA 510(k) clearance?

VIDAR BONE TRACK SYSTEM SOFTWARE received FDA 510(k) clearance on 2003-03-04, under 510(k) number K024171.

Who is the listed applicant for VIDAR BONE TRACK SYSTEM SOFTWARE?

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

What is the FDA product code for VIDAR BONE TRACK SYSTEM SOFTWARE?

The FDA product code for VIDAR BONE TRACK SYSTEM SOFTWARE is JAK.

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Other records listing Vidar Systems Corp. as applicant

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.

K130636TELERADPRO EDGE; TELERADPRO EDGE HD-CCDK130406DIAGNOSTICPRO EDGEK102476TELERADPROK093809VIDAR DENTAL FILM DIGITIZERK071193VIDAR VISION 3000 AND 4000 X-RAY SYSTEMSK070563VIDAR VISION 2000

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Related Devices (Code: JAK)

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

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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