Atlas FDA

Rush Medullary Pins

FDA 510(k) clearance K150626 · decided 2015-05-01

Clearance details

K-number
K150626
Device name
Rush Medullary Pins
Applicant
Zimmer, Inc.
Decision
Substantially Equivalent
Date received
2015-03-11
Decision date
2015-05-01
Days to decision
51 days
Clearance type
Traditional
Product code
HTY
Device class
2
Regulation number
888.3040
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Warsaw, IN, 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

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NEXGEN LPS-FLEX MOBILE AND LPS-MOBILE BEARING KNEE SYSTEM (P060037/S092)Zimmer, Inc.2024-12-12
NexGen® LPS-Flex LPS-Mobile Bearing Knee (P060037/S091)Zimmer, Inc.2024-07-05
NexGen® LPS-Flex / LPS Mobile Bearing Knee System (P060037/S090)Zimmer, Inc.2024-05-17
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NexGen® LPS-Flex/LPS Mobile Bearing Knee System (P060037/S088)Zimmer, Inc.2024-02-13