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FDA 510(k)

SPINOCAN(R) CONTINUOUS SPINAL TRAY

K-Number: K895192 · 1989-09-18

ApplicantBurron Medical, Inc.
Decision Date1989-09-18
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SPINOCAN(R) CONTINUOUS SPINAL TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Burron Medical, Inc.. It received FDA 510(k) clearance on 1989-09-18 under 510(k) number K895192. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPINOCAN(R) CONTINUOUS SPINAL TRAY?

SPINOCAN(R) CONTINUOUS SPINAL TRAY is a medical device that received FDA 510(k) clearance on 1989-09-18. The listed applicant is Burron Medical, Inc.. The 510(k) number is K895192.

When did SPINOCAN(R) CONTINUOUS SPINAL TRAY receive FDA 510(k) clearance?

SPINOCAN(R) CONTINUOUS SPINAL TRAY received FDA 510(k) clearance on 1989-09-18, under 510(k) number K895192.

Who is the listed applicant for SPINOCAN(R) CONTINUOUS SPINAL TRAY?

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

What is the FDA product code for SPINOCAN(R) CONTINUOUS SPINAL TRAY?

The FDA product code for SPINOCAN(R) CONTINUOUS SPINAL TRAY is CAZ.

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Other records listing Burron Medical, 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.

K902401CELSITE(TM) IMPLANTABLE DRUG DELIVERY SYSTEMK896422BURRON AMBULATORY DRUG DELIVERY SYSTEMK884235COMBITRANS DISPOSABLE PRESSURE TRANSDUCER KITK895191ANTI-THROMBOGENIC COATING FOR CATHETERSK884183BURRON TEFLON-COATED GUIDEWIREK882106PERFUSOR M SYRINGE PUMP

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Related Devices (Code: CAZ)

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.

K261372Profoject™ LOR SyringeCMT Health PTE., Ltd.K222341Arrow 0.2 Micron Flat Filter, GVSArrow International, LLCK210983BD Epilor SyringeBecton, Dickinson and CompanyK201356Plastic LOR SyringeJiangsu Caina Medical Co.,LtdK202699E-Cath STIM acc. TsuiPAJUNK GmbH MedizintechnologieK190345VPCPAJUNK GmbH Medizintechnologie

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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