Atlas FDA

BIOBUCK CEMENT RESTRICTOR

FDA 510(k) clearance K023680 · decided 2002-11-19

Clearance details

K-number
K023680
Device name
BIOBUCK CEMENT RESTRICTOR
Applicant
Smith & Nephew, Inc.
Decision
Substantially Equivalent
Date received
2002-11-01
Decision date
2002-11-19
Days to decision
18 days
Clearance type
Special
Product code
LZN
Device class
2
Regulation number
878.3300
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Memphis, TN, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Artisan Bone Plug, Universal Cement Restrictor (K220838)Howmedica Osteonics, Dba Stryker Orthopaedics2022-05-20
TORNIER CEMENT RESTRICTOR (K061824)Tornier2006-09-14
CEMSTOP CEMENT RESTRICTOR (K032685)Teknimed, S.A.2003-11-26
IMPRO VISE ABSORBABLE CEMENT FLOW RESTRICTOR (K011943)Kensey Nash Corp.2001-09-19
SYNPLUG (K010840)Isotis NV2001-04-20
CEMSTOP CEMENT RESTRICTOR (K993841)Encore Orthopedics, Inc.2000-05-04
SHUTTLE STOP (K000587)Isotis NV2000-05-04
OSTEONICS UNIVERSAL DISTAL CEMENT PLUG (K992462)Howmedica Osteonics Corp.1999-08-13
LINK CEMENT PLUG (K972411)Turnkey Intergration USA, Inc.1997-08-29
OSTEONICS TIBIAL TRAY SCREW HOLE PLUGS (K970779)Osteonics Corp.1997-05-09
ORTHOPLUG SOFT BONE DESIGN (K955632)Sunmed, Inc.1996-02-27
ORTHOPLUG HARD BONE DESIGN (K955631)Sunmed, Inc.1996-02-27

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
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R3 Delta Ceramic Hip System (P150030/S045)Smith & Nephew, Inc.2025-02-28
R3™ Delta Ceramic Acetabular System (P150030/S047)Smith & Nephew, Inc.2025-02-21
R3™ Delta Ceramic Acetabular System (P150030/S046)Smith & Nephew, Inc.2025-01-16
BIRMINGHAM HIP™ RESURFACING (BHR) SYSTEM (P040033/S039)Smith & Nephew, Inc.2025-01-10