FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

SYNTEC-TAICHUNG NON-STERILE DHS/DCS PLATE SYSTEM

K Number: K983873 · Decision Dec 30, 1998
Classifications
1
FEI Numbers
249
Registration Numbers
249
Same Product Code
403
Applicant Total
13
Review Days
58

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Basic Information

Device Name
SYNTEC-TAICHUNG NON-STERILE DHS/DCS PLATE SYSTEM
K Number
K983873
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Syntec Scientific Corp.
Date Received
November 2, 1998
Decision Date
December 30, 1998
Product Code
KTT
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
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

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Other Clearances by Syntec Scientific Corp.

K Number Device Name
K111189 SYNTEC DENTAL IMPLANT
K101971 SYNTEC OS SPINAL FIXATION SYSTEM
K092889 SYNTEC OSTEO-PLATE AND SCREW FIXATION
K090476 SYNTEC ORTHODONTIC MINI SCREW
K090839 MODIFICATION TO SYNTEC-TAICHUN NON-STERILE BONE PLATE AND SCREW IMPLANTS
K984602 SYNTEC-TAICHUNG NON-STERILE UNREAMED INTERLOCKING NAIL SYSTEM
K984364 SYNTEC-TAICHUNG NON-STERILE SMALL ORTHOPEDIC FIXATION SYSTEM, MODEL 71100, 294-300,400 & 292-730/820
K984543 SYNTEC-TAICHUNG NON-STERILE INTERLOCKING NAIL SYSTEM, MODEL:HUMERUS:256-000/280, FEMUR:274-000/870, TIBIA:249-300/420 25
K983988 SYNTEC-TAICHUNG NON-STERILE TITANIUM ALLOY MINI-PLATE
K983495 SYNTEC-TAICHUNG NON-STERILE BONE PLATE AND SCREW IMPLANTS, MODEL#'S 222020-248120, 240050-240980, 241130-246620, 4240420
Search all 13 clearances from Syntec Scientific Corp. →