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

T2 TIBIAL NAILING SYSTEM

K Number: K131365 · Decision Oct 10, 2013
Classifications
1
FEI Numbers
302
Registration Numbers
302
Same Product Code
528
Applicant Total
25
Review Days
150

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
T2 TIBIAL NAILING SYSTEM
K Number
K131365
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3020
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Trauma AG
Date Received
May 13, 2013
Decision Date
October 10, 2013
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 Stryker Trauma AG

K Number Device Name
K172210 ReUnion Reversible Fracture System (RFX), ReUnion Reverse Shoulder Arthroplasty System (RSA), ReUnion Total Shoulder Arthroplasty System (TSA)
K153154 Asnis JFX System
K151178 VariAx 2 Wrist Fusion System
K143138 AxSOS 3 Ti Locking Plate System
K140961 HOFFMANN LRF (LIMB RECONSTRUCTION FRAME) SYSTEM
K141992 VARIAX 2 SYSTEM
K141677 VARIAX ELBOW PLATING SYSTEM
K141204 VARIAX 2 ONE THIRD TUBULAR PLATING SYSTEM
K141121 AXSOS 3 TI LOCKING PLATE SYSTEM
K140565 VARIAX 2 COMPRESSION PLATING SYSTEM
Search all 25 clearances from Stryker Trauma AG →