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FDA 510(k)

SPINAL TOUCH

K-Number: K961212 · 1996-06-12

ApplicantFasstech
Decision Date1996-06-12
Product CodeKQX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SPINAL TOUCH is the device name listed in this FDA 510(k) record. The listed applicant is Fasstech. It received FDA 510(k) clearance on 1996-06-12 under 510(k) number K961212. The device is classified under product code KQX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPINAL TOUCH?

SPINAL TOUCH is a medical device that received FDA 510(k) clearance on 1996-06-12. The listed applicant is Fasstech. The 510(k) number is K961212.

When did SPINAL TOUCH receive FDA 510(k) clearance?

SPINAL TOUCH received FDA 510(k) clearance on 1996-06-12, under 510(k) number K961212.

Who is the listed applicant for SPINAL TOUCH?

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

What is the FDA product code for SPINAL TOUCH?

The FDA product code for SPINAL TOUCH is KQX.

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 Fasstech 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.

K063447INSIGHT DISCOVERYK033452CWAS 1000K023209INSIGHT MILLENNIUM IIIK011964INSIGHT MILLENNIUM PLUSK011983INSIGHT GENESISK990778INSIGHT MILLENNIUM

View all 9 devices →

Related Devices (Code: KQX)

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.

K011827ORTELIUS 800Orthoscan , Ltd.K971079INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWAREInterlogics, Inc.K9623773D-SPINESkill Technologies, Inc.K954647INCLINOMETERJ-Tech, Inc.K943929DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS)Greenleaf Medical Systems, Inc.K945630LARGE MUSCLE STRENGTH GAUGEJ-Tech, 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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