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FDA 510(k)

WHITESIDE BIOMECHANICS SPINAL SYSTEM

K-Number: K991678 · 1999-08-12

ApplicantWhiteside Biomechanics, Inc.
Decision Date1999-08-12
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

WHITESIDE BIOMECHANICS SPINAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Whiteside Biomechanics, Inc.. It received FDA 510(k) clearance on 1999-08-12 under 510(k) number K991678. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WHITESIDE BIOMECHANICS SPINAL SYSTEM?

WHITESIDE BIOMECHANICS SPINAL SYSTEM is a medical device that received FDA 510(k) clearance on 1999-08-12. The listed applicant is Whiteside Biomechanics, Inc.. The 510(k) number is K991678.

When did WHITESIDE BIOMECHANICS SPINAL SYSTEM receive FDA 510(k) clearance?

WHITESIDE BIOMECHANICS SPINAL SYSTEM received FDA 510(k) clearance on 1999-08-12, under 510(k) number K991678.

Who is the listed applicant for WHITESIDE BIOMECHANICS SPINAL SYSTEM?

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

What is the FDA product code for WHITESIDE BIOMECHANICS SPINAL SYSTEM?

The FDA product code for WHITESIDE BIOMECHANICS SPINAL SYSTEM is KWQ.

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Other records listing Whiteside Biomechanics, 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.

K033313QUATRO M FEMORAL COMPONENTK012800SYMMETRIC UNICOMPARTMENTAL KNEE SYSTEMK003618WHITESIDE BIOMECHANICS LOW PROFILE STAINLESS STEEL CABLE SYSTEM, MODEL BIO-1-1014K993903WHITESIDE BIOMECHANICS TITANIUM LOW-PROFILE CABLE, MODEL BIO-1-1013K981238BIPOLAR FEMORAL HEADK973261WHITESIDE BIOMECHANICS, INC. CERAMIC UNIPOLAR FEMORAL HEAD

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Related Devices (Code: KWQ)

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.

K262149corra® cervical plating systemCarlsmed, Inc.K261309Palisades™ Buttress Plate SystemBethesda Medical Devices, LLCK252776ARIES Anterior Cervical Plate SystemsZheJiang Decans Medical Devices Co., Ltd.K261112CastleLoc-P Anterior Cervical Plate SystemL&K BIOMED Co., Ltd.K260570corra™ cervical plating systemCarlsmed, Inc.K260697VyPlate™ Anterior Cervical Plate SystemVy Spine, LLC

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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