FDA 510(k) FDA class 1 Substantially Equivalent for Some Indications 🇺🇸 United States

BONE SUTURE FIXATION DEVICE

K Number: K880264 · Decision Mar 23, 1988
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
6
Applicant Total
95
Review Days
61

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Basic Information

Device Name
BONE SUTURE FIXATION DEVICE
K Number
K880264
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Orthopedic Systems, Inc.
Date Received
January 22, 1988
Decision Date
March 23, 1988
Product Code
HXY
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
HXY Brace, Drill

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K910031 PARK CITY SHOULDER POSITIONER
K903938 C FIT CUP
K892503 NUFFIELD TOTAL KNEE
K896678 SILICONE PLUG
K894283 COMPREHENSIVE SPINE MOTION ANALYZER
K890498 FREEMAN MODULAR HIP STEM RIDGED VERSION
K890331 FREEMAN TOTAL HIP SYSTEM RIDGED STEM
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