FDA 510(k)

LEVTECH COMPOSITE TRACTION TONGS

K-Number: K873693 · 1988-02-05

Decision Date1988-02-05

Product CodeHAX

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

LEVTECH COMPOSITE TRACTION TONGS is the device name listed in this FDA 510(k) record. The listed applicant is Levtech, Inc.. It received FDA 510(k) clearance on 1988-02-05 under 510(k) number K873693. The device is classified under product code HAX. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEVTECH COMPOSITE TRACTION TONGS?

LEVTECH COMPOSITE TRACTION TONGS is a medical device that received FDA 510(k) clearance on 1988-02-05. The listed applicant is Levtech, Inc.. The 510(k) number is K873693.

When did LEVTECH COMPOSITE TRACTION TONGS receive FDA 510(k) clearance?

LEVTECH COMPOSITE TRACTION TONGS received FDA 510(k) clearance on 1988-02-05, under 510(k) number K873693.

Who is the listed applicant for LEVTECH COMPOSITE TRACTION TONGS?

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

What is the FDA product code for LEVTECH COMPOSITE TRACTION TONGS?

The FDA product code for LEVTECH COMPOSITE TRACTION TONGS is HAX.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Levtech, Inc. as applicant

K910128LEVTECH TITANIUM BONE WIRE K901144LEVTECH BONE SCREW K874023LEVTECH CLAMP APPLIER K850039HALIFAX SPINAL CLAMP

Related Devices (Code: HAX)

K090733PMT HALO SYSTEMPmt Corp.K071173RESOLVE TONGS, SMALL/MEDIUM, RESOLVE TONGS, MEDIUM/LARGE, MODEL JT-200D, JT-100DOssur Americans (Formerly the Jerome Group)K051918RESOLVE OPEN BACK HALO RINGSJerome Medical K023959JEROME GLASS RINGThe Jerome Group, Inc.K003662SPINE WORKS COLLARSpine Works K980689FRIDDLE HALO SYSTEM, FRIDDLE MRI HALO SYSTEMFriddle'S Orthopedic Appliances, 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.