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FDA 510(k)

SPINAL SPECIALTIES NERVE BLOCK TRAY

K-Number: K960100 · 1996-04-24

ApplicantSpinal Specialties, Inc.
Decision Date1996-04-24
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SPINAL SPECIALTIES NERVE BLOCK TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Spinal Specialties, Inc.. It received FDA 510(k) clearance on 1996-04-24 under 510(k) number K960100. 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 SPINAL SPECIALTIES NERVE BLOCK TRAY?

SPINAL SPECIALTIES NERVE BLOCK TRAY is a medical device that received FDA 510(k) clearance on 1996-04-24. The listed applicant is Spinal Specialties, Inc.. The 510(k) number is K960100.

When did SPINAL SPECIALTIES NERVE BLOCK TRAY receive FDA 510(k) clearance?

SPINAL SPECIALTIES NERVE BLOCK TRAY received FDA 510(k) clearance on 1996-04-24, under 510(k) number K960100.

Who is the listed applicant for SPINAL SPECIALTIES NERVE BLOCK TRAY?

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

What is the FDA product code for SPINAL SPECIALTIES NERVE BLOCK TRAY?

The FDA product code for SPINAL SPECIALTIES NERVE BLOCK TRAY is CAZ.

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Other records listing Spinal Specialties, 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.

K960082DISCOGRAPHY KITK942863EPIDURAL NEEDLEK944029CONTINUOUS EPIDURAL ANESTHESIA TRAYK943319GERTIE MARX EPI-SPINAL TRAYK950820SPINAL SPECIALTIES PENCIL-POINT SPINAL NEEDLEK941343SPINAL ANESTHESIA TRAY

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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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