Cleared Special

K103433 - F20

K103433 is an FDA 510(k) clearance for F20, manufactured by Teknimed, S.A.. The device is a Class 2 Orthopedic device with product code NDN cleared through the Special 510(k) pathway after a 40-day FDA review.

K103433 · Teknimed, S.A. · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 2011
Decision
40d
Days
Class 2
Risk

K103433 is an FDA 510(k) clearance for the F20. Classified as Cement, Bone, Vertebroplasty (product code NDN), Class II - Special Controls.

Submitted by Teknimed, S.A. (Round Rock, US). The FDA issued a Cleared decision on January 3, 2011 after a review of 40 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 Teknimed, S.A. devices

FDA 510(k) Submission Details - K103433

510(k) Number K103433 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 24, 2010
Decision Date January 03, 2011
Days to Decision 40 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
82d faster than avg
Panel avg: 122d · This submission: 40d
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 K103433.
KYPHON XPEDE BONE CEMENT
K102397 · Medtronic · Feb 2011
ARTHROCARE PARALLAX CONTOUR VERTEBRAL AUGMENTATION DEVICE
K110183 · Arthrocare Corp. · Feb 2011
AVAMAX VERTEBRAL BALLOON
K103064 · Care Fusion · Jan 2011
PARALLAX CONTOUR VERTEBRAL AUGMENTATION DEVICE
K100479 · Arthrocare Corp. · Sep 2010
KYPH X HV-R BONE CEMENT
K093828 · Medtronic, Inc. · Aug 2010
AVAMAX VERTEBRAL BALLOON MODEL VBS1010, VBS1015, VBS1020
K093463 · Care Fusion · Feb 2010