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

TRILLIANT SURGICAL K-WIRES

K Number: K121008 · Decision Jun 4, 2012
Classifications
1
FEI Numbers
283
Registration Numbers
283
Same Product Code
203
Applicant Total
14
Review Days
62

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
TRILLIANT SURGICAL K-WIRES
K Number
K121008
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Trilliant Surgical, Ltd.
Date Received
April 3, 2012
Decision Date
June 4, 2012
Product Code
HTY
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
HTY Pin, Fixation, Smooth

Similar 510(k) Clearances

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

View all

Other Clearances by Trilliant Surgical, Ltd.

K Number Device Name
K172178 Minimally Invasive Bunion Plating System
K162354 Sniper Staple System
K160177 Gridlock Ankle Plating System
K153338 Tiger Cannulated Screw System
K130964 GRIDLOCK PLATING SYSTEM
K123525 GRIDLOCK PLATING SYSTEM
K122959 HAMMER TOE IMPLANT
K121452 GRIDLOCK PLATING SYSTEM
K111834 DISCO SUBTALAR IMPLANT
K112737 TIGER HEADLESS CANNULATED SCREWS
Search all 14 clearances from Trilliant Surgical, Ltd. →