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FDA 510(k)

RELIANCE POSTERIOR CERVICAL- THORACIC SYSTEM

K-Number: K122292 · 2012-10-24

ApplicantReliance Medical Systems, LLC
Decision Date2012-10-24
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

RELIANCE POSTERIOR CERVICAL- THORACIC SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Reliance Medical Systems, LLC. It received FDA 510(k) clearance on 2012-10-24 under 510(k) number K122292. 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 RELIANCE POSTERIOR CERVICAL- THORACIC SYSTEM?

RELIANCE POSTERIOR CERVICAL- THORACIC SYSTEM is a medical device that received FDA 510(k) clearance on 2012-10-24. The listed applicant is Reliance Medical Systems, LLC. The 510(k) number is K122292.

When did RELIANCE POSTERIOR CERVICAL- THORACIC SYSTEM receive FDA 510(k) clearance?

RELIANCE POSTERIOR CERVICAL- THORACIC SYSTEM received FDA 510(k) clearance on 2012-10-24, under 510(k) number K122292.

Who is the listed applicant for RELIANCE POSTERIOR CERVICAL- THORACIC SYSTEM?

The FDA 510(k) record lists Reliance Medical Systems, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RELIANCE POSTERIOR CERVICAL- THORACIC SYSTEM?

The FDA product code for RELIANCE POSTERIOR CERVICAL- THORACIC SYSTEM is KWP.

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Other records listing Reliance Medical Systems, LLC 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.

K202266Reliance Cervical IBF SystemK210874Reliance Spinal Screw SystemK183049Reliance Lumbar IBF SystemK173283Reliance Lumbar IBF SystemK173102Reliance Cervical IBF SystemK172489Reliance Cervical IBF System

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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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