Atlas FDA

PERIARTICULAR LOCKING PLATES AND SCREWS, MODEL 2358 SERIES

FDA 510(k) clearance K051098 · decided 2005-07-07

Clearance details

K-number
K051098
Device name
PERIARTICULAR LOCKING PLATES AND SCREWS, MODEL 2358 SERIES
Applicant
Zimmer, Inc.
Decision
Substantially Equivalent
Date received
2005-04-29
Decision date
2005-07-07
Days to decision
69 days
Clearance type
Traditional
Product code
HWC
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/S094)Zimmer, Inc.2025-04-01
NEXGEN LPS-FLEX MOBILE AND LPS-MOBILE BEARING KNEE SYSTEM (P060037/S092)Zimmer, Inc.2024-12-12
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NexGen® LPS-Flex / LPS Mobile Bearing Knee System (P060037/S090)Zimmer, Inc.2024-05-17
NexGen LPS-Flex/LPS Mobile Bearing Knee System (P060037/S089)Zimmer, Inc.2024-04-04
NexGen® LPS-Flex/LPS Mobile Bearing Knee System (P060037/S088)Zimmer, Inc.2024-02-13