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FDA 510(k)

Erisma® Deformity Spinal System; Erisma® Lp Spinal Fixation System

K-Number: K240872 · 2024-04-26

ApplicantClariance
Decision Date2024-04-26
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Erisma® Deformity Spinal System; Erisma® Lp Spinal Fixation System is the device name listed in this FDA 510(k) record. The listed applicant is Clariance. It received FDA 510(k) clearance on 2024-04-26 under 510(k) number K240872. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Erisma® Deformity Spinal System; Erisma® Lp Spinal Fixation System?

Erisma® Deformity Spinal System; Erisma® Lp Spinal Fixation System is a medical device that received FDA 510(k) clearance on 2024-04-26. The listed applicant is Clariance. The 510(k) number is K240872.

When did Erisma® Deformity Spinal System; Erisma® Lp Spinal Fixation System receive FDA 510(k) clearance?

Erisma® Deformity Spinal System; Erisma® Lp Spinal Fixation System received FDA 510(k) clearance on 2024-04-26, under 510(k) number K240872.

Who is the listed applicant for Erisma® Deformity Spinal System; Erisma® Lp Spinal Fixation System?

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

What is the FDA product code for Erisma® Deformity Spinal System; Erisma® Lp Spinal Fixation System?

The FDA product code for Erisma® Deformity Spinal System; Erisma® Lp Spinal Fixation System is NKB.

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.

NCT07414745MDT-0123 Japan StudyRECRUITING

Other records listing Clariance 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.

K243904Elegance® Anterior Cervical plateK243670Idys® LIFK241863Erisma® Lp Spinal Fixation System; Erisma® LP MISK240715Idys® C ZP 3DTiK220182Aggeris™-CK212562Idys-C ZP 3DTi

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Related Devices (Code: NKB)

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.

K260362QUATTRO Spinal system (Open Configuration); QUATTRO-GADGET Spinal system (MIS Configuration)MANTIZ Co., Ltd.K253943Tiger 2 SystemZavation Medical Products, LLCK261284Invictus® Small Stature Spinal Fixation System; Invictus® 2.0 Spinal Fixation SystemAlphatec Spine, Inc.K253802KHEIRON® Spinal Fixation System, including patient specific K-RODS.M.A.I.OK253045“Socko” Vimax Spinal Fixation SystemSocko Medical Co., Ltd.K251251ChanPin Pedicle Screw Spinal SystemChanpin Medtak Co., Ltd.

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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