Atlas FDA

Medussa-PL Cage

FDA 510(k) clearance K223654 · decided 2022-12-28

Clearance details

K-number
K223654
Device name
Medussa-PL Cage
Applicant
Medyssey USA, Inc.
Decision
Substantially Equivalent
Date received
2022-12-06
Decision date
2022-12-28
Days to decision
22 days
Clearance type
Special
Product code
MAX
Device class
2
Regulation number
888.3080
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Buffalo Grove, IL, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.