Atlas FDA

FMP METAL/METAL ACETABULAR INSERT, 499-28,449-34, 499-38

FDA 510(k) clearance K070221 · decided 2007-04-04

Clearance details

K-number
K070221
Device name
FMP METAL/METAL ACETABULAR INSERT, 499-28,449-34, 499-38
Applicant
Encore Medical L.P.
Decision
Substantially Equivalent
Date received
2007-01-24
Decision date
2007-04-04
Days to decision
70 days
Clearance type
Traditional
Product code
KWA
Device class
3
Regulation number
888.3330
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Austin, TX, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.