Atlas FDA

CEMENTRALIZER DISTAL STEM CENTRALIZER

FDA 510(k) clearance K951930 · decided 1995-07-11

Clearance details

K-number
K951930
Device name
CEMENTRALIZER DISTAL STEM CENTRALIZER
Applicant
Depuy, Inc.
Decision
Substantially Equivalent
Date received
1995-04-05
Decision date
1995-07-11
Days to decision
97 days
Clearance type
Traditional
Product code
LZN
Device class
2
Regulation number
878.3300
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Warsaw, IN, US
Third-party review
No
Expedited review
No

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IMPRO VISE ABSORBABLE CEMENT FLOW RESTRICTOR (K011943)Kensey Nash Corp.2001-09-19
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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

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
ATTUNE™ Revision Rotating Platform (RP) Knee System (P830055/S346)Depuy, Inc.2025-12-18
LCS Total Knee System (P830055/S355)Depuy, Inc.2025-12-15
LCS® Total Knee System (P830055/S354)Depuy, Inc.2025-12-11
LCS® Total Knee System (P830055/S353)Depuy, Inc.2025-12-09
LCS® Total Knee System (P830055/S352)Depuy, Inc.2025-11-26
LCS® Total Knee System (P830055/S350)Depuy, Inc.2025-09-26
LCS® Total Knee System (P830055/S349)Depuy, Inc.2025-09-09
LCS Total Knee System (P830055/S348)Depuy, Inc.2025-08-29