Atlas FDA

EVOLUTION HIP SYSTEM

FDA 510(k) clearance K896105 · decided 1989-12-29

Clearance details

K-number
K896105
Device name
EVOLUTION HIP SYSTEM
Applicant
Dow Corning Wright
Decision
Substantially Equivalent for Some Indications
Date received
1989-10-20
Decision date
1989-12-29
Days to decision
70 days
Clearance type
Traditional
Product code
KWL
Device class
2
Regulation number
888.3360
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Arlington, 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
REMEDY POLY+PLUS SNAP FIT Acetabular Cup (K262290)Osteoremedies, LLC2026-07-24
Prostalac Hip System, SmartSet V+G Dual Antibiotic Bone Cement (K260536)Depuy Ireland UC2026-05-15
OsteoRemedies Hip Spacer System (K253675)Osteoremedies, LLC2025-12-23
InterSpace GV Hip Spacer (K252326)Tecres S.P.A.2025-08-06
Synicem Hip Spacer; Synicem Knee Spacer; Synicem Shoulder Spacer (K242865)Biocomposites, Ltd.2025-06-12
COPAL® exchange G hip spacer; COPAL® G+V (K234028)Heraeus Medical GmbH2024-02-15
UHR Bipolar Implants, Restoration GAP II Implants (K222632)Howmedica Osteonics Corp., Dba Stryker Orthopaedics2022-10-21
OsteoRemedies Hip Spacer System (K192995)Osteoremedies, LLC2020-01-10
REMEDY Acetabular Cup (K191981)Osteoremedies, LLC2019-08-23
REMEDY PLUS Hip Spacer, UNITE PLUS Bone Cement (K172906)Osteoremedies, LLC2018-08-29
Remedy Acetabular Cup (K173967)Osteoremedies, LLC2018-02-22
Evolve UniPolar Head (K143184)Signature Orthopaedics Pty, Ltd.2015-03-17

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
WHITESIDE EPS(TM) FEMORAL HIP PROSTHESIS (P880076/S001)Dow Corning Wright1991-06-17