FDA 510(k)

CLEARVIEW PLUS BONE AND VERTEBRAL BODY BIOPSY NEEDLES

K-Number: K022169 · 2002-07-25

Decision Date2002-07-25

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

CLEARVIEW PLUS BONE AND VERTEBRAL BODY BIOPSY NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Parallax Medical, Inc.. It received FDA 510(k) clearance on 2002-07-25 under 510(k) number K022169. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEARVIEW PLUS BONE AND VERTEBRAL BODY BIOPSY NEEDLES?

CLEARVIEW PLUS BONE AND VERTEBRAL BODY BIOPSY NEEDLES is a medical device that received FDA 510(k) clearance on 2002-07-25. The listed applicant is Parallax Medical, Inc.. The 510(k) number is K022169.

When did CLEARVIEW PLUS BONE AND VERTEBRAL BODY BIOPSY NEEDLES receive FDA 510(k) clearance?

CLEARVIEW PLUS BONE AND VERTEBRAL BODY BIOPSY NEEDLES received FDA 510(k) clearance on 2002-07-25, under 510(k) number K022169.

Who is the listed applicant for CLEARVIEW PLUS BONE AND VERTEBRAL BODY BIOPSY NEEDLES?

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

What is the FDA product code for CLEARVIEW PLUS BONE AND VERTEBRAL BODY BIOPSY NEEDLES?

The FDA product code for CLEARVIEW PLUS BONE AND VERTEBRAL BODY BIOPSY NEEDLES is KNW.

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Other records listing Parallax Medical, Inc. as applicant

K033230TRACERS TA BONE CEMENT OPACIFIER, MODEL TCR-TA K023445TRACERS BONE CEMENT OPACIFIER K011206PARALLAX BONE AND VERTEBRAL BODY BIOPSY AND INFUSION NEEDLES K994022PARALLAX CRANIOSET K991893PARALLAX TRACER RADIOPAQUE PARTICLES

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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.