Atlas FDA

FUSON BONE PLUG, RADIOPAQUE

FDA 510(k) clearance K800142 · decided 1980-02-19

Clearance details

K-number
K800142
Device name
FUSON BONE PLUG, RADIOPAQUE
Applicant
Zimmer, Inc.
Decision
Substantially Equivalent
Date received
1980-01-21
Decision date
1980-02-19
Days to decision
29 days
Clearance type
Traditional
Product code
JDS
Device class
2
Regulation number
888.3030
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Walker, MI, 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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Auxein Nailing System (K192003)Auxein Medical Private Limited2020-06-10
WIN Flexible Nail System (K193533)Biomet, Inc.2020-02-20
CONVENTUS PHS SYSTEM (K141737)Conventus Orthopaedics, Inc.2015-04-08
CHINA NAILS AND ACCESSORIES (K123948)Smith & Nephew, Inc.2013-03-14
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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