Atlas FDA

Persona Partial Knee Tibial Cut Guide 5 Deg Left Medial Right Lateral, Persona Partial Knee Tibial Cut Guide 5 Deg Right Medial Left Lateral, Persona Partial Knee 2MM Tibial Recutter Left Medial Right Lateral, Persona Partial Knee 2MM Tibial Recutter Right Medial Left Lateral, Persona Partial Knee Tibial Drill

FDA 510(k) clearance K200151 · decided 2020-03-17

Clearance details

K-number
K200151
Device name
Persona Partial Knee Tibial Cut Guide 5 Deg Left Medial Right Lateral, Persona Partial Knee Tibial Cut Guide 5 Deg Right Medial Left Lateral, Persona Partial Knee 2MM Tibial Recutter Left Medial Right Lateral, Persona Partial Knee 2MM Tibial Recutter Right Medial Left Lateral, Persona Partial Knee Tibial Drill
Applicant
Zimmer, Inc.
Decision
Substantially Equivalent
Date received
2020-01-22
Decision date
2020-03-17
Days to decision
55 days
Clearance type
Traditional
Product code
HSX
Device class
2
Regulation number
888.3520
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Warsaw, IN, 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
Tahoe Unicondylar Knee System with TiNbN Overcoat (K260796)Shalby Advanced Technologies, Inc. Dba Consensus Orthopedics2026-04-02
Cambridge Partial Knee (K251771)Signature Orthopaedics Pty, Ltd.2025-12-16
Persona Partial Knee (K251834)Zimmer Biomet2025-08-15
MOTO Partial Knee System Extension (K251618)Medacta International S.A.2025-07-24
Arthrex iBalance Partial Knee System (K251453)Arthrex, Inc.2025-07-01
ACTIFY™ Unicondylar Knee System (K241260)Globus Medical, Inc.2024-12-06
JOURNEY II Unicompartmental Knee System (JOURNEY II UK) (K242711)Smith & Nephew, Inc.2024-10-30
OvertureTi Knee Resurfacing SystemTM (K242746)Overture Orthopaedics2024-10-07
TRIBRID® Unicompartmental Knee System (K232114)Kyocera Medical Technologies, Inc.2024-04-04
Uni Knee Resurfacing System (K221292)Overture Resurfacing, Inc.2023-03-10
TLC Unicompartmental Knee System (K212870)Signature Orthopaedics Pty, Ltd.2022-06-16
Restoris Multi-Compartmental Knee System (K220930)Mako Surgical Corp.2022-06-02

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
NexGen© LPSFlex/ LPS Mobile Bearing Knee System (P060037/S095)Zimmer, Inc.2025-08-18
NexGen© LPSFlex/LPS Mobile Bearing Knee System (P060037/S093)Zimmer, Inc.2025-04-09
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
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
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