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

ENSPLINT TM BONE SCREW

K Number: K080778 · Decision Jul 10, 2008
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
9
Review Days
113

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Basic Information

Device Name
ENSPLINT TM BONE SCREW
K Number
K080778
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sonoma Orthopedic Products, Inc.
Date Received
March 19, 2008
Decision Date
July 10, 2008
Product Code
HWC
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
HWC Screw, Fixation, Bone

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Other Clearances by Sonoma Orthopedic Products, Inc.

K Number Device Name
K161371 Sonoma Fifth Metatarsal Repair System
K142945 Sonoma Fibula Repair System
K111550 SONOMA FASTRAC CLAVICLE FRACTURE REPAIR DEVICE MODEL SONOMA FASTRAC XXYYY(X=DIA, YYY=LENGTH- IN MM)
K100112 SOMONA CWG CLAVICLE FRACTURE REPAIR DEVICE MODEL SONOMA CWG XYYY(X=DIA, YYY=LENGTH-IN MM)
K092110 WAVEON FRACTURE REPAIR SYSTEM (WAVEON RX)
K090304 WAVEON WRX BONE FIXATION SYSTEM
K081832 ENSPLINTCMX CLAVICLE PIN
K071809 ENSPLINTRX BONE FIXATION SYSTEM