FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Affixus Retrograde Femoral Nailing System

K Number: K253566 · Decision Mar 12, 2026
Classifications
1
FEI Numbers
302
Registration Numbers
302
Same Product Code
528
Applicant Total
376
Review Days
115

Basic Information

Device Name
Affixus Retrograde Femoral Nailing System
K Number
K253566
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3020
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zimmer, Inc.
Date Received
November 17, 2025
Decision Date
March 12, 2026
Product Code
HSB
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HSB Rod, Fixation, Intramedullary And Accessories

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HSB), ordered by most recent decision date.

View all

Other Clearances by Zimmer, Inc.

K Number Device Name
K261683 Augment Off-Axis Instrument System
K260831 Z1 Hip System
K251840 Zimmer® Persona® Personalized Knee System
K260182 Avenir® Müller Stem; Avenir Complete™ Hip System
K253592 Zimmer Biomet Reverse Shoulder Prosthesis (Alliance Humeral Bearings, Identity Humeral Trays, Comprehensive Reverse Humeral Trays, Comprehensive Reverse 32mm Glenospheres and Adapter)
K253189 Persona the Personalized Knee System (Persona Porous Plasma Spray PPS Femurs)
K252623 G7® Revision Acetabular System
K251098 Identity Revision Humeral Stems
K251906 Z1 Hip System
K250848 Identity Shoulder System
Search all 376 clearances from Zimmer, Inc. →