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FDA 510(k)

MULTIPLE NONPOWERED NEUROSURGICAL INSTRUMENT

K-Number: K902818 · 1990-09-20

ApplicantRuggles Corp.
Decision Date1990-09-20
Product CodeHBG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MULTIPLE NONPOWERED NEUROSURGICAL INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Ruggles Corp.. It received FDA 510(k) clearance on 1990-09-20 under 510(k) number K902818. The device is classified under product code HBG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIPLE NONPOWERED NEUROSURGICAL INSTRUMENT?

MULTIPLE NONPOWERED NEUROSURGICAL INSTRUMENT is a medical device that received FDA 510(k) clearance on 1990-09-20. The listed applicant is Ruggles Corp.. The 510(k) number is K902818.

When did MULTIPLE NONPOWERED NEUROSURGICAL INSTRUMENT receive FDA 510(k) clearance?

MULTIPLE NONPOWERED NEUROSURGICAL INSTRUMENT received FDA 510(k) clearance on 1990-09-20, under 510(k) number K902818.

Who is the listed applicant for MULTIPLE NONPOWERED NEUROSURGICAL INSTRUMENT?

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

What is the FDA product code for MULTIPLE NONPOWERED NEUROSURGICAL INSTRUMENT?

The FDA product code for MULTIPLE NONPOWERED NEUROSURGICAL INSTRUMENT is HBG.

Related Clinical Trials

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.

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Other records listing Ruggles Corp. 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.

K903485TITANIUM MESHK902819LAMINECTOMY ROGEURK902850ZEPPELIN INSTRUMENTSK893415TRANS-ORAL DEPTH GAUGE

Related Devices (Code: HBG)

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.

K252696LEGACYPhasor Health, LLCK153587Taps for Resorbable ScrewsSynthes (USA) Products, LLCK162884SpineGuard DSG Zavation Screw SystemSpineguard S.A.K160129MRII Cranial Drill and AccessoriesMri Interventions, Inc.K122456MRII CRAINIAL DRILLMri Interventions, Inc.K022712HAND DRILL, MODEL 11-9901-7Medical Design, LLC

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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