Cleared Traditional

K082848 - NUBIC AND RABEA DEVICES

K082848 is the FDA 510(k) clearance for NUBIC AND RABEA DEVICES by Signus Medizintechnik GmbH. It is a Class 2 Orthopedic device (product code ODP) cleared through the Traditional 510(k) pathway after a 298-day FDA review.

K082848 · Signus Medizintechnik GmbH · Orthopedic device
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Jul 2009
Decision
298d
Days
Class 2
Risk

K082848 is an FDA 510(k) clearance for the NUBIC AND RABEA DEVICES. Classified as Intervertebral Fusion Device With Bone Graft, Cervical (product code ODP), Class II - Special Controls.

Submitted by Signus Medizintechnik GmbH (Chesterland, US). The FDA issued a Cleared decision on July 24, 2009 after a review of 298 days - an extended review cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3080 - the FDA orthopedic device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. 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 Signus Medizintechnik GmbH devices

Submission Details

510(k) Number K082848 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 29, 2008
Decision Date July 24, 2009
Days to Decision 298 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
176d slower than avg
Panel avg: 122d · This submission: 298d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code ODP Intervertebral Fusion Device With Bone Graft, Cervical
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3080
Definition Intended To Stabilize Cervical Spinal Segment To Promote Fusion In Order To Restrict Motion And Decrease Pain Using Bone Graft.
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Orthopedic devices follow this clearance model.

Regulatory Peers - ODP Intervertebral Fusion Device With Bone Graft, Cervical

All 220
Devices cleared under the same product code (ODP) and FDA review panel - the closest regulatory comparables to K082848.
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K081611 · Nuvasive, Inc. · Oct 2008
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