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FDA 510(k)

ARTHRONET BLACKLINE 2 AND 3 PIECE ARTHROSCOPIC BLADES, MODELS 123, 133, 153, 163, 173 AND 183

K-Number: K023777 · 2002-12-11

ApplicantArthronet Medical, Inc.
Decision Date2002-12-11
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTHRONET BLACKLINE 2 AND 3 PIECE ARTHROSCOPIC BLADES, MODELS 123, 133, 153, 163, 173 AND 183 is the device name listed in this FDA 510(k) record. The listed applicant is Arthronet Medical, Inc.. It received FDA 510(k) clearance on 2002-12-11 under 510(k) number K023777. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHRONET BLACKLINE 2 AND 3 PIECE ARTHROSCOPIC BLADES, MODELS 123, 133, 153, 163, 173 AND 183?

ARTHRONET BLACKLINE 2 AND 3 PIECE ARTHROSCOPIC BLADES, MODELS 123, 133, 153, 163, 173 AND 183 is a medical device that received FDA 510(k) clearance on 2002-12-11. The listed applicant is Arthronet Medical, Inc.. The 510(k) number is K023777.

When did ARTHRONET BLACKLINE 2 AND 3 PIECE ARTHROSCOPIC BLADES, MODELS 123, 133, 153, 163, 173 AND 183 receive FDA 510(k) clearance?

ARTHRONET BLACKLINE 2 AND 3 PIECE ARTHROSCOPIC BLADES, MODELS 123, 133, 153, 163, 173 AND 183 received FDA 510(k) clearance on 2002-12-11, under 510(k) number K023777.

Who is the listed applicant for ARTHRONET BLACKLINE 2 AND 3 PIECE ARTHROSCOPIC BLADES, MODELS 123, 133, 153, 163, 173 AND 183?

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

What is the FDA product code for ARTHRONET BLACKLINE 2 AND 3 PIECE ARTHROSCOPIC BLADES, MODELS 123, 133, 153, 163, 173 AND 183?

The FDA product code for ARTHRONET BLACKLINE 2 AND 3 PIECE ARTHROSCOPIC BLADES, MODELS 123, 133, 153, 163, 173 AND 183 is HRX.

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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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