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

UNITY ALPHA SYSTEM

K Number: K062820 · Decision Mar 15, 2007
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
12
Review Days
176

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Basic Information

Device Name
UNITY ALPHA SYSTEM
K Number
K062820
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bonutti Research, Inc.
Date Received
September 20, 2006
Decision Date
March 15, 2007
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 Bonutti Research, Inc.

K Number Device Name
K161628 JAS Pulse(TM) Ultrasonic Therapy
K093078 UNITY ULTRASONIC SYSTEM WITH PLLA ANCHORS
K090175 UNITY BETA PLLA SYSTEM
K082906 UNITY BETA ANCHOR SYSTEM
K060283 TRANSET SYSTEM
K052799 MULTITAK 6.0 MM ABSORBABLE ANCHOR SYSTEM
K033717 TRANSET FRACTURE FIXATION SYSTEM
K013177 MULTITAK SUTURE SNAP SYSTEM
K012465 MULTITAK SPLINTER 3.0 MM RESORBABLE ANCHOR
K010479 MULTITAK CONICAL TIP BONE SOFT TISSUE SUTURE ANCHOR
Search all 12 clearances from Bonutti Research, Inc. →