Atlas FDA

HOWMEDICA OSTEONICS RADIAL HEAD PROTHESIS

FDA 510(k) clearance K001385 · decided 2000-07-27

Clearance details

K-number
K001385
Device name
HOWMEDICA OSTEONICS RADIAL HEAD PROTHESIS
Applicant
Howmedica Osteonics Corp.
Decision
Substantially Equivalent
Date received
2000-05-02
Decision date
2000-07-27
Days to decision
86 days
Clearance type
Traditional
Product code
KWI
Device class
2
Regulation number
888.3170
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Rutherford, NJ, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
Trident Alumina Insert (625-0T-XXX); Osteonics® ABC/Trident® System (P000013/S027)Howmedica Osteonics Corp.2025-09-17
Trident Acetabular System: Trident Alumina Inserts (P000013/S026)Howmedica Osteonics Corp.2025-05-23
Trident® Acetabular System (P000013/S025)Howmedica Osteonics Corp.2024-03-08
Trident(R), ABC(R) (P000013/S024)Howmedica Osteonics Corp.2024-01-23
Trident Ceramic System (P000013/S021)Howmedica Osteonics Corp.2023-12-20
Trident(R), ABC(R) (P000013/S023)Howmedica Osteonics Corp.2023-12-19
Trident®, ABC® (P000013/S022)Howmedica Osteonics Corp.2023-09-27
Trident Acetabular System: Trident Alumina Inserts (P000013/S020)Howmedica Osteonics Corp.2022-04-01