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FDA 510(k)

PILOT POSTERIOR LUMBAR PLATING SYSTEM

K-Number: K061364 · 2006-09-05

ApplicantLife Spine
Decision Date2006-09-05
Product CodeMNH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PILOT POSTERIOR LUMBAR PLATING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Life Spine. It received FDA 510(k) clearance on 2006-09-05 under 510(k) number K061364. The device is classified under product code MNH. It was reviewed by the OR advisory panel. Product code MNH falls under the category of ENT, which includes ear, nose, and throat diagnostic and surgical devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PILOT POSTERIOR LUMBAR PLATING SYSTEM?

PILOT POSTERIOR LUMBAR PLATING SYSTEM is a medical device that received FDA 510(k) clearance on 2006-09-05. The listed applicant is Life Spine. The 510(k) number is K061364.

When did PILOT POSTERIOR LUMBAR PLATING SYSTEM receive FDA 510(k) clearance?

PILOT POSTERIOR LUMBAR PLATING SYSTEM received FDA 510(k) clearance on 2006-09-05, under 510(k) number K061364.

Who is the listed applicant for PILOT POSTERIOR LUMBAR PLATING SYSTEM?

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

What is the FDA product code for PILOT POSTERIOR LUMBAR PLATING SYSTEM?

The FDA product code for PILOT POSTERIOR LUMBAR PLATING SYSTEM is MNH. This falls under the ENT category.

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Other records listing Life Spine 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.

K182470Plateau Spacer SystemK160169The Life Spine Subtalar Implant SystemK131077LIFE SPINE PLATEAU SPACER SYSTEMK123373NAUTILUS SPINAL SYSTEMK120998SOLSTICE CROSS CONNECTORK111953NAUTILUS SPINAL SYSTEM

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Related Devices (Code: MNH)

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.

K162066Reliance Spinal Screw SystemReliance Medical Systems, LLCK162801CastleLoc Spinal Fixation SystemL&K BIOMED Co., Ltd.K162143FixxSure® X-LinkInnovasis, Inc.K161151Spinal fixation systemCanwell Medical Co., Ltd.K162189ANAX™ 5.5 Spinal SystemU&I CorporationK151362HC Spinal SystemHung Chun Bio-S 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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