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FDA 510(k)

VTI ADULT DISPOSABLE SKULL PIN, MODEL 22000; VTI SKULL SCREW, MODEL 22001

K-Number: K002990 · 2000-11-06

Decision Date2000-11-06
Product CodeHBL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VTI ADULT DISPOSABLE SKULL PIN, MODEL 22000; VTI SKULL SCREW, MODEL 22001 is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Technology Incorporated. It received FDA 510(k) clearance on 2000-11-06 under 510(k) number K002990. The device is classified under product code HBL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VTI ADULT DISPOSABLE SKULL PIN, MODEL 22000; VTI SKULL SCREW, MODEL 22001?

VTI ADULT DISPOSABLE SKULL PIN, MODEL 22000; VTI SKULL SCREW, MODEL 22001 is a medical device that received FDA 510(k) clearance on 2000-11-06. The listed applicant is Vascular Technology Incorporated. The 510(k) number is K002990.

When did VTI ADULT DISPOSABLE SKULL PIN, MODEL 22000; VTI SKULL SCREW, MODEL 22001 receive FDA 510(k) clearance?

VTI ADULT DISPOSABLE SKULL PIN, MODEL 22000; VTI SKULL SCREW, MODEL 22001 received FDA 510(k) clearance on 2000-11-06, under 510(k) number K002990.

Who is the listed applicant for VTI ADULT DISPOSABLE SKULL PIN, MODEL 22000; VTI SKULL SCREW, MODEL 22001?

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

What is the FDA product code for VTI ADULT DISPOSABLE SKULL PIN, MODEL 22000; VTI SKULL SCREW, MODEL 22001?

The FDA product code for VTI ADULT DISPOSABLE SKULL PIN, MODEL 22000; VTI SKULL SCREW, MODEL 22001 is HBL.

Related Clinical Trials

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.

Other records listing Vascular Technology Incorporated 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.

View all 11 devices →

Related Devices (Code: HBL)

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.

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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