Atlas FDA

CITATION TMZF HA STEM

FDA 510(k) clearance K993768 · decided 2000-01-21

Clearance details

K-number
K993768
Device name
CITATION TMZF HA STEM
Applicant
Howmedica Osteonics Corp.
Decision
Substantially Equivalent
Date received
1999-11-08
Decision date
2000-01-21
Days to decision
74 days
Clearance type
Traditional
Product code
MEH
Device class
2
Regulation number
888.3353
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Rutherford, NJ, 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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Recalls involving this device

RecordFirmDate
Citation TMZF HA 132 degrees Neck Angle, V40 Hip Stem - Right Size #3: catalog # 6265-5113 recall (Z-1317-2014)Stryker Howmedica Osteonics Corp.2014-04-02
Citation TMZF HA Hip Stem - LT. Hip stems are single use devices intended for cementless f recall (Z-1374-2009)Stryker Howmedica Osteonics Corp.2009-07-22
Citation TMZF HA Hip Stem - LT. Hip stems are single use devices intended for cementless f recall (Z-1375-2009)Stryker Howmedica Osteonics Corp.2009-07-22
Citation TMZF HA Hip Stem - LT. Hip stems are single use devices intended for cementless f recall (Z-1376-2009)Stryker Howmedica Osteonics Corp.2009-07-22
Citation TMZF HA Hip Stem - RT. Hip stems are single use devices intended for cementless f recall (Z-1377-2009)Stryker Howmedica Osteonics Corp.2009-07-22
Citation TMZF HA Hip Stem - RT. Hip stems are single use devices intended for cementless f recall (Z-1378-2009)Stryker Howmedica Osteonics Corp.2009-07-22
Citation TMZF HA Hip Stem - RT. Hip stems are single use devices intended for cementless f recall (Z-1379-2009)Stryker Howmedica Osteonics Corp.2009-07-22
Citation TMZF HA Hip Stem - RT. Hip stems are single use devices intended for cementless f recall (Z-1380-2009)Stryker Howmedica Osteonics Corp.2009-07-22
Citation TMZF HA Hip Stem - RT. Hip stems are single use devices intended for cementless f recall (Z-1381-2009)Stryker Howmedica Osteonics Corp.2009-07-22
Short Citation TMZF HA Hip Stem - Right; Hydroxylapatite Coated, Titanium Plasma Spray; V4 recall (Z-1382-2009)Stryker Howmedica Osteonics Corp.2009-07-22
Citation TMZF HA Hip Stem Right (Femoral Hip Prosthesis) Catalog No. 6265-5116 recall (Z-0349-03)Howmedica Osteonics Corp2002-12-19
Citation TMZF HA Hip Stem Left (Femoral Hip Prosthesis) Catalog No. 6265-5106 recall (Z-0350-03)Howmedica Osteonics Corp2002-12-19

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