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

AOS TIBIAL NAIL

K Number: K070444 · Decision Jun 14, 2007
Classifications
1
FEI Numbers
302
Registration Numbers
302
Same Product Code
528
Applicant Total
23
Review Days
119

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
AOS TIBIAL NAIL
K Number
K070444
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3020
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Advanced Orthopaedic Solutions, Inc.
Date Received
February 15, 2007
Decision Date
June 14, 2007
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 Advanced Orthopaedic Solutions, Inc.

K Number Device Name
K202489 AOS Fibonacci Lower Extremity Plating System – AOS Proximal Tibia Plating System
K202099 AOS Galileo™ Trochanteric Nail System
K191598 AOS ES Retrograde Femoral Nail
K160409 AOS Anterolateral Proximal Humeral Plate
K143204 AOS Clavicle Intramedullary Device
K141912 AOS SMALL BONE EXTERNAL FIXATION, THREADED HALF PINS, AOS SMALL BONE EXTERNAL FIXATION, CARBON FIBER RODS, AOS SMALL BON
K141228 AOS 6.5MM CAPTURED, FULLY THREADED CANCELLOUS SCREW
K133081 TROCHANTERIC NAILS AND ES TROCHANTERIC NAILS, HUMERAL NAISL, TIBIAL NAILS, ANTEGRADE FEMORAL NAILS, RETROGRADE FEMORAL N
K132005 RETROGRADE FEMORAL NAIL
K123569 ANTEGRADE FEMORAL NAIL
Search all 23 clearances from Advanced Orthopaedic Solutions, Inc. →