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FDA 510(k)

CANCELLOUS SCREW

K-Number: K862990 · 1986-10-29

ApplicantOrthopedic Systems, Inc.
Decision Date1986-10-29
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CANCELLOUS SCREW is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Systems, Inc.. It received FDA 510(k) clearance on 1986-10-29 under 510(k) number K862990. 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 CANCELLOUS SCREW?

CANCELLOUS SCREW is a medical device that received FDA 510(k) clearance on 1986-10-29. The listed applicant is Orthopedic Systems, Inc.. The 510(k) number is K862990.

When did CANCELLOUS SCREW receive FDA 510(k) clearance?

CANCELLOUS SCREW received FDA 510(k) clearance on 1986-10-29, under 510(k) number K862990.

Who is the listed applicant for CANCELLOUS SCREW?

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

What is the FDA product code for CANCELLOUS SCREW?

The FDA product code for CANCELLOUS SCREW is HRX.

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Other records listing Orthopedic Systems, Inc. as applicant

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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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