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FDA 510(k)

CADENCE SPINAL FIXATION SYSTEM

K-Number: K022374 · 2002-09-24

ApplicantSulzer Spine-Tech
Decision Date2002-09-24
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CADENCE SPINAL FIXATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Sulzer Spine-Tech. It received FDA 510(k) clearance on 2002-09-24 under 510(k) number K022374. 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 CADENCE SPINAL FIXATION SYSTEM?

CADENCE SPINAL FIXATION SYSTEM is a medical device that received FDA 510(k) clearance on 2002-09-24. The listed applicant is Sulzer Spine-Tech. The 510(k) number is K022374.

When did CADENCE SPINAL FIXATION SYSTEM receive FDA 510(k) clearance?

CADENCE SPINAL FIXATION SYSTEM received FDA 510(k) clearance on 2002-09-24, under 510(k) number K022374.

Who is the listed applicant for CADENCE SPINAL FIXATION SYSTEM?

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

What is the FDA product code for CADENCE SPINAL FIXATION SYSTEM?

The FDA product code for CADENCE SPINAL FIXATION SYSTEM is KWP.

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Other records listing Sulzer Spine-Tech 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.

K020344RPX TITANIUM CEMNT RESTRICTORK020196MODIFICATION TO SILHOUETTE SPINAL FIXATION SYSTEMK012173DEVICE MODIFICATION OF SILHOUETTE SPINDAL FIXATION SYSTEMK012305MODIFICATION TO: TRINICA ANTERIOR CERVICAL PLATE SYSTEMK993067SILHOUETTE SPINAL FIXATION SYSTEMK992276MODIFICATION TO SILHOUETTE SPINAL FIXATION SYSTEM

View all 7 devices →

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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