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FDA 510(k)

PARALLAX ACRYLIC RESIN CARTRIDGE WITH TRACERS-TA

K-Number: K060425 · 2006-07-12

ApplicantArthrocare Corp.
Decision Date2006-07-12
Product CodeNDN
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PARALLAX ACRYLIC RESIN CARTRIDGE WITH TRACERS-TA is the device name listed in this FDA 510(k) record. The listed applicant is Arthrocare Corp.. It received FDA 510(k) clearance on 2006-07-12 under 510(k) number K060425. The device is classified under product code NDN. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARALLAX ACRYLIC RESIN CARTRIDGE WITH TRACERS-TA?

PARALLAX ACRYLIC RESIN CARTRIDGE WITH TRACERS-TA is a medical device that received FDA 510(k) clearance on 2006-07-12. The listed applicant is Arthrocare Corp.. The 510(k) number is K060425.

When did PARALLAX ACRYLIC RESIN CARTRIDGE WITH TRACERS-TA receive FDA 510(k) clearance?

PARALLAX ACRYLIC RESIN CARTRIDGE WITH TRACERS-TA received FDA 510(k) clearance on 2006-07-12, under 510(k) number K060425.

Who is the listed applicant for PARALLAX ACRYLIC RESIN CARTRIDGE WITH TRACERS-TA?

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

What is the FDA product code for PARALLAX ACRYLIC RESIN CARTRIDGE WITH TRACERS-TA?

The FDA product code for PARALLAX ACRYLIC RESIN CARTRIDGE WITH TRACERS-TA is NDN.

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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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