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FDA 510(k)

VERTETRAC

K-Number: K771988 · 1979-02-01

ApplicantBallert Orthopedic Corp.
Decision Date1979-02-01
Product CodeHST
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VERTETRAC is the device name listed in this FDA 510(k) record. The listed applicant is Ballert Orthopedic Corp.. It received FDA 510(k) clearance on 1979-02-01 under 510(k) number K771988. The device is classified under product code HST. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERTETRAC?

VERTETRAC is a medical device that received FDA 510(k) clearance on 1979-02-01. The listed applicant is Ballert Orthopedic Corp.. The 510(k) number is K771988.

When did VERTETRAC receive FDA 510(k) clearance?

VERTETRAC received FDA 510(k) clearance on 1979-02-01, under 510(k) number K771988.

Who is the listed applicant for VERTETRAC?

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

What is the FDA product code for VERTETRAC?

The FDA product code for VERTETRAC is HST.

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 Ballert Orthopedic Corp. 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.

K780617EQUALIZER

Related Devices (Code: HST)

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.

K162702Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression TableStl International, Inc.K110858LO-BAK TRAXRoland F Berthiaume, DCK984190BACK-ON-TRAC, MODEL 101BOTBack-On-Track, Inc.K872121K AND D HOME TRACTJoseph A. Kott, M.D.K870212ARTHROSCOPIC SHOULDER HOLDERDyonics, Inc.K870125EXTREMITY ELEVATOROrthopedic Systems, 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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