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FDA 510(k)

ARTHROSCOPIC RETRACTORS AND GRASPERS

K-Number: K925884 · 1993-03-04

ApplicantArthrex, Inc.
Decision Date1993-03-04
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTHROSCOPIC RETRACTORS AND GRASPERS is the device name listed in this FDA 510(k) record. The listed applicant is Arthrex, Inc.. It received FDA 510(k) clearance on 1993-03-04 under 510(k) number K925884. 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 ARTHROSCOPIC RETRACTORS AND GRASPERS?

ARTHROSCOPIC RETRACTORS AND GRASPERS is a medical device that received FDA 510(k) clearance on 1993-03-04. The listed applicant is Arthrex, Inc.. The 510(k) number is K925884.

When did ARTHROSCOPIC RETRACTORS AND GRASPERS receive FDA 510(k) clearance?

ARTHROSCOPIC RETRACTORS AND GRASPERS received FDA 510(k) clearance on 1993-03-04, under 510(k) number K925884.

Who is the listed applicant for ARTHROSCOPIC RETRACTORS AND GRASPERS?

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

What is the FDA product code for ARTHROSCOPIC RETRACTORS AND GRASPERS?

The FDA product code for ARTHROSCOPIC RETRACTORS AND GRASPERS is HRX.

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Related Devices (Code: HRX)

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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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