FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

MODIFIED FREEMAN REVISION ACETABULAR CUP

K Number: K902111 · Decision Aug 22, 1990
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
113
Applicant Total
26
Review Days
105

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Basic Information

Device Name
MODIFIED FREEMAN REVISION ACETABULAR CUP
K Number
K902111
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
888.3330
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Turnkey Intergration USA, Inc.
Date Received
May 9, 1990
Decision Date
August 22, 1990
Product Code
KWA
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KWA Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)

Similar 510(k) Clearances

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Other Clearances by Turnkey Intergration USA, Inc.

K Number Device Name
K991405 OMNI-FIX, HUMERAL NAIL
K990523 B2C, ESPACE REVISION CUP SYSTEM
K990307 OMNI-FIX, NAIL SYSTEM
K972411 LINK CEMENT PLUG
K970284 ARTOS, DIPLOS SYSTEM
K970084 LINK CERCLAGE WIRE SYSTEM
K953653 LUBINUS SP II HIP SYSTEM
K943986 LINK ENDO MODEL REVISION CUP
K951355 LINK SADDLE PROTHESIS
K950397 SYSTEM 22 VALVE
Search all 26 clearances from Turnkey Intergration USA, Inc. →