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FDA 510(k)

LAMINECTOMY ROGEUR

K-Number: K902819 · 1990-08-09

ApplicantRuggles Corp.
Decision Date1990-08-09
Product CodeLXH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LAMINECTOMY ROGEUR is the device name listed in this FDA 510(k) record. The listed applicant is Ruggles Corp.. It received FDA 510(k) clearance on 1990-08-09 under 510(k) number K902819. The device is classified under product code LXH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAMINECTOMY ROGEUR?

LAMINECTOMY ROGEUR is a medical device that received FDA 510(k) clearance on 1990-08-09. The listed applicant is Ruggles Corp.. The 510(k) number is K902819.

When did LAMINECTOMY ROGEUR receive FDA 510(k) clearance?

LAMINECTOMY ROGEUR received FDA 510(k) clearance on 1990-08-09, under 510(k) number K902819.

Who is the listed applicant for LAMINECTOMY ROGEUR?

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 LAMINECTOMY ROGEUR?

The FDA product code for LAMINECTOMY ROGEUR is LXH.

Related Clinical Trials

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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 MESHK902818MULTIPLE NONPOWERED NEUROSURGICAL INSTRUMENTK902850ZEPPELIN INSTRUMENTSK893415TRANS-ORAL DEPTH GAUGE

Related Devices (Code: LXH)

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.

K192873SX-One MicroKnifeSonex Health, Inc.K101609SELF RETAINING SOFT TISSUE RETRACTORKoros USA, Inc.K001507MICROPERFORATION INSTRUMENTSmith & Nephew, Inc.K952495ANCHORS AWAY SOFT TISSUE ATTACHMENT SYSTEMOrthopedic Systems, Inc.K943873ORTHOMET ANATOMICALLY GUIDED CARPAL TUNNEL RELEASE SYOrthomet, Inc.K944188SPINAL MARKERLeibinger L.P.

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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