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FDA 510(k)

ARTHROSCOPIC SURGERY BLADES DY-3440, 3443, 3444

K-Number: K901735 · 1990-06-20

ApplicantMicro-Aire Surgical Instruments, Inc.
Decision Date1990-06-20
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTHROSCOPIC SURGERY BLADES DY-3440, 3443, 3444 is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Aire Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1990-06-20 under 510(k) number K901735. 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 SURGERY BLADES DY-3440, 3443, 3444?

ARTHROSCOPIC SURGERY BLADES DY-3440, 3443, 3444 is a medical device that received FDA 510(k) clearance on 1990-06-20. The listed applicant is Micro-Aire Surgical Instruments, Inc.. The 510(k) number is K901735.

When did ARTHROSCOPIC SURGERY BLADES DY-3440, 3443, 3444 receive FDA 510(k) clearance?

ARTHROSCOPIC SURGERY BLADES DY-3440, 3443, 3444 received FDA 510(k) clearance on 1990-06-20, under 510(k) number K901735.

Who is the listed applicant for ARTHROSCOPIC SURGERY BLADES DY-3440, 3443, 3444?

The FDA 510(k) record lists Micro-Aire Surgical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTHROSCOPIC SURGERY BLADES DY-3440, 3443, 3444?

The FDA product code for ARTHROSCOPIC SURGERY BLADES DY-3440, 3443, 3444 is HRX.

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Other records listing Micro-Aire Surgical Instruments, Inc. 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.

K904949A.O. SYNTHES,TAP(REPLACEMENT)VARIOUS MODEL NUMBERSK903713OSTEOTOME MODEL NUMBERS 2500-228 & 2500-229K902676MICROGUARD, ORTHOPEDIC PIN PROTECTORSK903650OSCILLATING SAW BLADES # SO-305,MO-305 AND ZO-305K903664MICRO-AIRE WIRE PASS AND CRANIOTOME DRILLK901967DENDIA WERK BURS AND CUTTING DISCS

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Related Devices (Code: HRX)

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.

K260203Fule Vertebroplasty Balloon CatheterBeijing Fule Science & Technology Development Co., Ltd.K254103HOPKINS Telescopes for ArthroscopyKarl Storz SE & CO. KGK252790Digital ClarusScope System and Digital NeuroPEN SystemClarus Medical, LLCK253523Freedom DS™ Decompression SystemSpinal SimplicityK252546VantageTM Lumbar Decompression KitAllevion Medical, LLCK253217MiiS Horus Arthroscope (EJA 100); MiiS Horus Endoscope Display System -Tablet (EDS 500); MiiS Horus Endoscope Display System -Video Box (EVS 700)Medimaging Integrated Solution, Inc (Miis)

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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