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

CORTICELLOUS BONE SCREW

K Number: K953198 · Decision Nov 24, 1995
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
12
Review Days
141

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Basic Information

Device Name
CORTICELLOUS BONE SCREW
K Number
K953198
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Hayes Medical, Inc.
Date Received
July 6, 1995
Decision Date
November 24, 1995
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 Hayes Medical, Inc.

K Number Device Name
K070061 36MM COCR FEMORAL HEAD AND 36MM ACETABULAR INSERT
K062383 UNISYN HA PLASMA MODULAR HIP
K060635 CONSENSUS ACETABULAR SHELL SYSTEM
K030151 CONSENSUS HIP SYSTEM, UNISYN HIP SYSTEM
K030205 CONSENSUS UNIPOLAR HEAD, COCR
K021466 CONSENSUS ACETABULAR INSERT, CROSS-LINKED POLYETHYLENE
K020153 CONSENSUS ACETABLAR SHELL, TI COATED
K003649 TRITON HIP SYSTEM
K001456 CONSENSUS KNEE SYSTEM
K983004 CONSENSUS FEMORAL COMPONENT, POROUS, COCR/TI
Search all 12 clearances from Hayes Medical, Inc. →