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FDA 510(k)

ACUFEX ARTHROSCOPIC SHOULDER GUIDE SYSTEM

K-Number: K940481 · 1994-05-06

ApplicantAcufex Microsurgical, Inc.
Decision Date1994-05-06
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACUFEX ARTHROSCOPIC SHOULDER GUIDE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Acufex Microsurgical, Inc.. It received FDA 510(k) clearance on 1994-05-06 under 510(k) number K940481. 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 ACUFEX ARTHROSCOPIC SHOULDER GUIDE SYSTEM?

ACUFEX ARTHROSCOPIC SHOULDER GUIDE SYSTEM is a medical device that received FDA 510(k) clearance on 1994-05-06. The listed applicant is Acufex Microsurgical, Inc.. The 510(k) number is K940481.

When did ACUFEX ARTHROSCOPIC SHOULDER GUIDE SYSTEM receive FDA 510(k) clearance?

ACUFEX ARTHROSCOPIC SHOULDER GUIDE SYSTEM received FDA 510(k) clearance on 1994-05-06, under 510(k) number K940481.

Who is the listed applicant for ACUFEX ARTHROSCOPIC SHOULDER GUIDE SYSTEM?

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

What is the FDA product code for ACUFEX ARTHROSCOPIC SHOULDER GUIDE SYSTEM?

The FDA product code for ACUFEX ARTHROSCOPIC SHOULDER GUIDE SYSTEM is HRX.

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Other records listing Acufex Microsurgical, 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.

K961555ACUFEX TAG BIOABSORBABLE ANCHORSK961853PROLINE FAST PASS ARTHOSCOPIC NEEDLE PASSERK954246ACUFEX ENDOFIX ABSORBABLE INTERFERENCE SCREWK952535ACUFEX ENDOBUTTON TAPEK953276ACUFEX TAG DELIVERY SYSTEMK953459ACUFEX TAG ANCHOR

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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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