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FDA 510(k)

DISCOGRAPHY KIT

K-Number: K960082 · 1996-03-21

ApplicantSpinal Specialties, Inc.
Decision Date1996-03-21
Product CodeIZG
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DISCOGRAPHY KIT 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 1996-03-21 under 510(k) number K960082. The device is classified under product code IZG. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISCOGRAPHY KIT?

DISCOGRAPHY KIT is a medical device that received FDA 510(k) clearance on 1996-03-21. The listed applicant is Spinal Specialties, Inc.. The 510(k) number is K960082.

When did DISCOGRAPHY KIT receive FDA 510(k) clearance?

DISCOGRAPHY KIT received FDA 510(k) clearance on 1996-03-21, under 510(k) number K960082.

Who is the listed applicant for DISCOGRAPHY KIT?

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 DISCOGRAPHY KIT?

The FDA product code for DISCOGRAPHY KIT is IZG.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K960100SPINAL SPECIALTIES NERVE BLOCK TRAYK942863EPIDURAL NEEDLEK944029CONTINUOUS EPIDURAL ANESTHESIA TRAYK943319GERTIE MARX EPI-SPINAL TRAYK950820SPINAL SPECIALTIES PENCIL-POINT SPINAL NEEDLEK941343SPINAL ANESTHESIA TRAY

View all 8 devices →

Related Devices (Code: IZG)

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.

K960146G.E. STERILE DISPOSABLE RADIOGRAPHIC CONTRAST TRAYGE Medical SystemsK913436PXI PNEUMATIC COMPRESSION PADDLEBrotherston/PxiK920393MU125M MOBILE X-RAY SYSTEMShimadzu Medical SystemsK910503DISCOGRAPHY KITB. Braun of America, Inc.K903808AMSIS RDS, RADIOGRAPHIC DISCOGRAPHY KITAdvanced Med/Surg, Inc.K892659ELECTRODELCAOldelft Corp. of America

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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