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FDA 510(k)

ARTHROSCOPIC SHOULDER HOLDER

K-Number: K870212 · 1987-02-20

ApplicantDyonics, Inc.
Decision Date1987-02-20
Product CodeHST
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTHROSCOPIC SHOULDER HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Dyonics, Inc.. It received FDA 510(k) clearance on 1987-02-20 under 510(k) number K870212. The device is classified under product code HST. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHROSCOPIC SHOULDER HOLDER?

ARTHROSCOPIC SHOULDER HOLDER is a medical device that received FDA 510(k) clearance on 1987-02-20. The listed applicant is Dyonics, Inc.. The 510(k) number is K870212.

When did ARTHROSCOPIC SHOULDER HOLDER receive FDA 510(k) clearance?

ARTHROSCOPIC SHOULDER HOLDER received FDA 510(k) clearance on 1987-02-20, under 510(k) number K870212.

Who is the listed applicant for ARTHROSCOPIC SHOULDER HOLDER?

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

What is the FDA product code for ARTHROSCOPIC SHOULDER HOLDER?

The FDA product code for ARTHROSCOPIC SHOULDER HOLDER is HST.

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Other records listing Dyonics, 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.

K900070MODIFIED USES OF THE ARTHROSCOPIC SURGICAL SYSTEMK896416DYONICS SHOULDER PORTAL SYSTEMK893136SURGI-PAK FOR ARTHROSCOPIC ACROMIOPLASTYK890665MODIFIED CANNULA, TROCAR AND OBTURATOR ACCESSORIESK894728DYONICS DISPOSABLE ARTHROSCOPIC SURGICAL KNIFEK892062PS3500 ARTHROSCOPIC SURGICAL SYSTEM

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Related Devices (Code: HST)

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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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