Cleared Special

K072496 - MODIFICATION TO SPACE CPSXL BONE CEMENT

K072496 is an FDA 510(k) clearance for MODIFICATION TO SPACE CPSXL BONE CEMENT, manufactured by Dfine, Inc.. The device is a Class 2 Orthopedic device with product code NDN cleared through the Special 510(k) pathway after a 30-day FDA review.

K072496 · Dfine, Inc. · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 2007
Decision
30d
Days
Class 2
Risk

K072496 is an FDA 510(k) clearance for the MODIFICATION TO SPACE CPSXL BONE CEMENT. Classified as Cement, Bone, Vertebroplasty (product code NDN), Class II - Special Controls.

Submitted by Dfine, Inc. (San Jose, US). The FDA issued a Cleared decision on October 5, 2007 after a review of 30 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3027 - the FDA orthopedic device regulatory framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Dfine, Inc. devices

FDA 510(k) Submission Details - K072496

510(k) Number K072496 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 05, 2007
Decision Date October 05, 2007
Days to Decision 30 days
Submission Type Special
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
92d faster than avg
Panel avg: 122d · This submission: 30d
Pathway characteristics
Modification to existing cleared device.

NDN Device Classification - Class 2, Special Controls

Product Code NDN Cement, Bone, Vertebroplasty
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3027
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 - NDN Cement, Bone, Vertebroplasty

All 57
Devices cleared under the same product code (NDN) and FDA review panel - the closest regulatory comparables to K072496.
MESH FENESTRATED INTRODUCER NEEDLE (MESH INTRODUCER NEEDLE)
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K072118 · Stryker Corp. · Dec 2007
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ARCUATE VERTEBRAL AUGMENTATION SYSTEM
K070527 · Medtronic Sofamor Danek · May 2007
ARCUATE VERTEBRAL AUGMENTATION SYSTEM
K063248 · Medtronic Sofamor Danek · Mar 2007
CONFIDENCE FENESTRATED INTRODUCER NEEDLE
K063067 · Disc-O-Tech Medical Technologies, Ltd. · Nov 2006