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

SYNFIX-LR SPACER

K Number: K072253 · Decision Oct 12, 2007
Classifications
1
FEI Numbers
253
Registration Numbers
253
Same Product Code
200
Applicant Total
18
Review Days
59

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Basic Information

Device Name
SYNFIX-LR SPACER
K Number
K072253
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Synthes Spine Co.Lp
Date Received
August 14, 2007
Decision Date
October 12, 2007
Product Code
OVD
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
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

Similar 510(k) Clearances

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

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Other Clearances by Synthes Spine Co.Lp

K Number Device Name
K121852 SYNTHES ZERO-P VARIABLE ANGLE (VA)
K112459 SYNTHES ZERO-P
K112068 SYNTHES ZERO-P VARIABLE ANGLE (VA)
K103320 SYNTHES XRL
K081568 ANTEGRA-T
K080020 ARCOFIX
K072981 SYNTHES ZERO-P
K072434 SYNTHES OC FUSION AND SYNAPSE SYSTEMS
K070573 SYNAPSE SYSTEM
K062083 SYNFIX -LR
Search all 18 clearances from Synthes Spine Co.Lp →