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

INTERPHALANGEAL FLEXIBLE STABILIZING ROD SYSTEM

K Number: K022887 · Decision Nov 26, 2002
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
20
Applicant Total
27
Review Days
88

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Basic Information

Device Name
INTERPHALANGEAL FLEXIBLE STABILIZING ROD SYSTEM
K Number
K022887
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3720
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Osteomed Corp.
Date Received
August 30, 2002
Decision Date
November 26, 2002
Product Code
KWH
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
KWH Prosthesis, Toe, Constrained, Polymer

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KWH), ordered by most recent decision date.

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Other Clearances by Osteomed Corp.

K Number Device Name
K151021 OsteoMed Cannulated Screw System
K022277 OSTEOMED CRANIAL FLAP FIXATION SYSTEM
K022886 METATARSOPHALANGEAL FLEXIBLE STABILIZING ROD SYSTEM
K023260 1.2MM OSTEOMED AUTO-DRIVE SCREW SYSTEM
K013618 INTRAORAL MANDIBULAR DISTRACTION SYSTEM
K021618 OSA RIGID INTERNAL FIXATION SYSTEM
K012486 OSTEOMED BIORESORBABLE FIXATION SYSTEM
K010964 AUTO-DRIVE LAG SCREW SYSTEM
K010783 2.0/2.4 CANNULATED SCREW SYSTEM
K990944 OSTEOMED INTRAORAL DISTRACTION SYSTEM
Search all 27 clearances from Osteomed Corp. →