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FDA 510(k)

HARRINGTON SPINAL ELEVATOR

K-Number: K781449 · 1978-09-27

ApplicantOrthopedic Equipment Co., Inc.
Decision Date1978-09-27
Product CodeGEG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HARRINGTON SPINAL ELEVATOR is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Equipment Co., Inc.. It received FDA 510(k) clearance on 1978-09-27 under 510(k) number K781449. The device is classified under product code GEG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HARRINGTON SPINAL ELEVATOR?

HARRINGTON SPINAL ELEVATOR is a medical device that received FDA 510(k) clearance on 1978-09-27. The listed applicant is Orthopedic Equipment Co., Inc.. The 510(k) number is K781449.

When did HARRINGTON SPINAL ELEVATOR receive FDA 510(k) clearance?

HARRINGTON SPINAL ELEVATOR received FDA 510(k) clearance on 1978-09-27, under 510(k) number K781449.

Who is the listed applicant for HARRINGTON SPINAL ELEVATOR?

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

What is the FDA product code for HARRINGTON SPINAL ELEVATOR?

The FDA product code for HARRINGTON SPINAL ELEVATOR is GEG.

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 Orthopedic Equipment Co., 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.

K834035UNIVERSAL SELF-ALIGNING ACETABULAR COMK841189OEC/REZAIAN SPINAL FIXATORK800530SCHLEIN TRI-SURFACE ANKLEK781445SPREADERK790247TOURNIQUET TEST GAGEK790209FILTER SYSTEM, ALTNER DISPOSABLE

View all 45 devices →

Related Devices (Code: GEG)

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.

K891899ELEVATORS, VARIOUS TYPESZinnanti Surgical Instruments, Inc.K891894ELEVATORS-COTTLE,MCKENTY,GOLDMAN,JOSEPH,CONVERSEZinnanti Surgical Instruments, Inc.K890365SEPTUM ELEVATORKinetic Medical ProductsK890230LIGATURE NEEDLESKinetic Medical ProductsK890253SURGICAL ELEVATORKinetic Medical ProductsK8724911.1 TWIST DRILLS AND 1.2 CORTICAL DRILLSMicro-Aire Surgical Instruments, Inc.

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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