FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

PROXIMAL INTERPHALANGEAL JOINT IMPLANT

K Number: K802342 · Decision Oct 14, 1981
Classifications
1
FEI Numbers
227
Registration Numbers
227
Same Product Code
562
Applicant Total
11
Review Days
383

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Basic Information

Device Name
PROXIMAL INTERPHALANGEAL JOINT IMPLANT
K Number
K802342
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3350
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Sutter Biomedical, Inc.
Date Received
September 26, 1980
Decision Date
October 14, 1981
Product Code
JDI
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
JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

Similar 510(k) Clearances

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Other Clearances by Sutter Biomedical, Inc.

K Number Device Name
K875249 SUTTER PHALANGEAL CAP
K870200 SUTTER FINGER JOINT PROSTHESIS
K861983 SUTTER LESSER METATARSAL CAP
K850274 SUTTER CPM 9000 -NONMEASURING EXERCISE EQUIPMENT
K830974 SUTTER CPM 5000
K830649 SUTTER CPM 2000
K823539 SUTTER CPM
K820813 LESSER METATARSAL PHALANG. JOINT PROSTH
K820083 SUTTER CPM
K812691 SILICONE IMPLANTS
Search all 11 clearances from Sutter Biomedical, Inc. →