Cleared Traditional

K051320 - SATELLITE SPINAL SYSTEM (FDA 510(k) Clearance)

Class III device cleared through the 510(k) pathway via substantial equivalence to a legally marketed predicate.

K051320 · Medtronic Sofamor Danek · Orthopedic device
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Sep 2005
Decision
112d
Days
Class 3
Risk

K051320 is an FDA 510(k) clearance for the SATELLITE SPINAL SYSTEM. Classified as Intervertebral Fusion Device With Bone Graft, Solid-sphere, Lumbar (product code NVR), Class III - Premarket Approval.

Submitted by Medtronic Sofamor Danek (Memphis, US). The FDA issued a Cleared decision on September 9, 2005 after a review of 112 days - within the typical 510(k) review window.

This device falls under the Orthopedic FDA review panel. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: High-complexity regulatory submission. High regulatory complexity profile. This clearance follows a standard predicate-based equivalence path within the Orthopedic review framework, consistent with the majority of Class II 510(k) submissions.

View all Medtronic Sofamor Danek devices

Submission Details

510(k) Number K051320 FDA.gov
FDA Decision Cleared Substantially Equivalent - Abbreviated 510(k) (SESU)
Date Received May 20, 2005
Decision Date September 09, 2005
Days to Decision 112 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
10d faster than avg
Panel avg: 122d · This submission: 112d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code NVR Intervertebral Fusion Device With Bone Graft, Solid-sphere, Lumbar
Device Class Class 3 - Premarket Approval
Definition Intended To Be Inserted Between The Vertebral Bodies Into The Disc Space From L3 To S1 To Provide Stabilization And To Help Promote Intervertebral Body Fusion. To Be Used With Bone Graft, For Holding Bone Parts In Alignment While They Heal. Not Intended For Use In Motion-sparing, Non-fusion Procedures, Helps Promote Intervertebral Body Fusion, Please Reference: Https://www.federalregister.gov/documents/2023/03/30/2023-06566/medical-devices-orthopedic-devices-classification-of-spinal-spheres-for-use-in-intervertebral-fusion.
What this classification means

Class III devices typically require Premarket Approval (PMA) with clinical evidence. Clearance through 510(k) for Class III devices is granted only when substantial equivalence to a valid predicate can be established.