Atlas FDA

CORIN TRINITY ACETABULAR SYSTEM ECIMA LINERS

FDA 510(k) clearance K111481 · decided 2012-02-06

Clearance details

K-number
K111481
Device name
CORIN TRINITY ACETABULAR SYSTEM ECIMA LINERS
Applicant
Corin USA
Decision
Substantially Equivalent
Date received
2011-05-27
Decision date
2012-02-06
Days to decision
255 days
Clearance type
Traditional
Product code
OQI
Device class
2
Regulation number
888.3353
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Tampa, FL, 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.

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EPORE® XO cup system (K252451)Implantcast GmbH2026-04-24
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E-XPE Acetabular Components and U-Motion II Acetabular Cup (K172833)United Orthopedic Corporation2018-06-12
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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
Cormet Hip Resurfacing System (P050016/S012)Corin USA2020-07-17
CORMET HIP RESURFACING SYSTEM (P050016/S011)Corin USA2016-12-21
CORMET HIP RESURFACING SYSTEM (P050016/S010)Corin USA2014-04-03
CORMET HIP RESURFACING SYSTEM (P050016/S009)Corin USA2013-03-22
CORMET HIP RESURFACING SYSTEM (P050016/S008)Corin USA2011-11-10
CORMET HIP RESURFACING SYSTEM (P050016/S007)Corin USA2011-01-13
CORMET HIP RESURFACING SYSTEM (P050016/S006)Corin USA2009-12-31
CORMET HIP RESURFACING SYSTEM (P050016/S005)Corin USA2009-12-03