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

SYNTHES SYNEX SPACER SYSTEM

K Number: K003836 · Decision May 29, 2001
Classifications
1
FEI Numbers
222
Registration Numbers
222
Same Product Code
276
Applicant Total
11
Review Days
168

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Basic Information

Device Name
SYNTHES SYNEX SPACER SYSTEM
K Number
K003836
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Synthes
Date Received
December 12, 2000
Decision Date
May 29, 2001
Product Code
MQP
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
MQP Spinal Vertebral Body Replacement Device

Similar 510(k) Clearances

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

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Other Clearances by Synthes

K Number Device Name
K123723 SYNTHES MATRIXNEURO CRANIAL PLATING SYSTEM
K122455 SYNTHES SMALL EXTERNAL FIXATION SYSTEM, SYNTHES LARGE EXTERNAL FIXATION SYSTEM
K113071 SYNTHECEL DURA REPLACEMENT DEVICES
K110604 VBB SYSTEM
K093772 SYNTHES STERNAL FIXATION SYSTEM
K013072 CHRONOS TRICALCIUM PROSPHATE (CHRONOS TCP)
K020602 SYNTHES PILON PLATE
K010108 USS-LINE EXTENSION
K003061 SYNTHES USS (10.0MM SIDE OPENING SCREWS)
K982732 SYNTHES (USA) DISTAL RADIUS PLATE SYSTEM (DRPS)
Search all 11 clearances from Synthes →