FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MODIFICATION TO SYNTHES (USA) REAMER IRRIGATOR ASPIRATOR (RIA) SYSTEM

K Number: K013527 · Decision Dec 21, 2001
Classifications
1
FEI Numbers
354
Registration Numbers
354
Same Product Code
13
Applicant Total
402
Review Days
59

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Basic Information

Device Name
MODIFICATION TO SYNTHES (USA) REAMER IRRIGATOR ASPIRATOR (RIA) SYSTEM
K Number
K013527
Device Class
FDA class 1
Clearance Type
Special
Regulation Number
888.4540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Synthes (Usa)
Date Received
October 23, 2001
Decision Date
December 21, 2001
Product Code
HTO
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
HTO Reamer

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Other Clearances by Synthes (Usa)

K Number Device Name
K131984 SYNTHES SYNSONIC ULNA NAIL
K111667 SYNTHES SUPRAPATELLAR INSERTION INSTRUMENTS
K111540 SYNTHES 3.5MM LCP CLAVICLE PLATE SYSTEM
K110789 SYNTHES STERNAL ZIPFIX SYSTEM
K103002 SYNTHES MULTILOC PROXIMAL HUMERAL NAILING SYSTEM
K103243 2.4MM VA-LCP INTERCARPAL FUSION SYSTEM
K102656 SYNTHES DENTOALVEOLAR BONE FIXATION SYSTEM
K093299 SYNTHES ORTHODONTIC BONE ANCHOR SYSTEM
K102694 2.4MM VA-LCP DORSAL DISTAL RADIUS PLATES
K100776 SYNTHES 2.4 MM/2.7 MM VARIABLE ANGLE LCP FOREFOOT/MIDFOOT SYSTEM
Search all 402 clearances from Synthes (Usa) →