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

S2 FEMORAL NAIL

K Number: K022461 · Decision Aug 22, 2002
Classifications
1
FEI Numbers
302
Registration Numbers
302
Same Product Code
528
Applicant Total
13
Review Days
27

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
S2 FEMORAL NAIL
K Number
K022461
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3020
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Howmedica Osteonics
Date Received
July 26, 2002
Decision Date
August 22, 2002
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 Howmedica Osteonics

K Number Device Name
K120578 ACCOLADE II HIP STEM
K102019 RESTORATION ACETABULAR WEDGE AUGMENTS
K063423 TRIATHLON CS (CONDYLAR STABILIZING) LIPPED INSERT
K033258 BONESAVE BONE VOID FILLER
K032855 STRYKER SPINE MAPS SYSTEM
K031702 REFLEX ANTERIOR CERVICAL PLATE SYSTEM
K031435 BONESOURCE BVF
K031217 GMRS PRESS FIT STEMS WITH PUREFIX HA
K022160 XIA SPINAL SYSTEM
K013772 MODIFICATION TO HOFFMANN II MICRO EXTERNAL FIXATION SYSTEM
Search all 13 clearances from Howmedica Osteonics →