510(k) K982390

Device
CONCISE COMPRESSION HIP SCREW SYSTEM (STERILE)
Applicant
Wrightmedicaltechnologyinc
510(k) number
K982390
Product code
KTW
Decision
Substantially Equivalent (SESE)
Decision date
1998-09-14
Date received
1998-07-09
Regulation
888.3030
Classification name
Appliance, Fixation, Nail/Blade/Plate Combination, Single Component
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
LYNNE WITKOWSKI
Address
5677 Airline Rd. Arlington TN US 38002 38002

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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K012634REPROCESSED EXTERNAL FIXATION DEVICEAlliance Medical, Inc.2002-06-24
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K011815SYNTHES LCP PROXIMAL HUMERUS PLATESSynthes (Usa)2001-09-06
K011458SYNTHES STRAIGHT WRIST FUSION PLATE, 170MMSynthes (Usa)2001-08-02
K010321MODULAR FOOT SYSTEM - 2.7 MM MODULESynthes (Usa)2001-05-02
K001614STRYKER TRAUMA PELVIC SETHowmedica Osteonics Corp.2000-08-04