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FDA 510(k)

A HOOK DRIVER

K-Number: K820660 · 1982-03-19

ApplicantTwin City Surgical, Inc.
Decision Date1982-03-19
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

A HOOK DRIVER is the device name listed in this FDA 510(k) record. The listed applicant is Twin City Surgical, Inc.. It received FDA 510(k) clearance on 1982-03-19 under 510(k) number K820660. The device is classified under product code KWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A HOOK DRIVER?

A HOOK DRIVER is a medical device that received FDA 510(k) clearance on 1982-03-19. The listed applicant is Twin City Surgical, Inc.. The 510(k) number is K820660.

When did A HOOK DRIVER receive FDA 510(k) clearance?

A HOOK DRIVER received FDA 510(k) clearance on 1982-03-19, under 510(k) number K820660.

Who is the listed applicant for A HOOK DRIVER?

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

What is the FDA product code for A HOOK DRIVER?

The FDA product code for A HOOK DRIVER is KWP.

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 Twin City Surgical, 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.

K870767THE (CROM) TESTERK861632SIMS CHAIRK830585ANVIL RETRACTORK820659A CALIPERK813067SPINAL WRENCH

Related Devices (Code: KWP)

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.

K133094CERTEX OCT SPINAL IMPLANT SYSTEMX-Spine Systems, Inc.K132504TIGER OCCIPITAL-CERVICAL-THORACIC SPINAL FIXATION SYSTEMCorelink, LLCK132900MARAUDER CERVICAL-THORACIC SPINAL FIXATION SYSTEMIntelligent Implant Systems, LLCK131427LOTUSSpinal Elements, Inc.K132332MOUNTAINEER OCT SPINAL SYSTEMMedos International SARLK131156LANX SPINAL FIXATION SYSTEMLanx, 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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