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

AESCULAP RESORBABLE PIN, MODEL FR735

K Number: K070178 · Decision Apr 30, 2007
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
219
Applicant Total
18
Review Days
101

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Basic Information

Device Name
AESCULAP RESORBABLE PIN, MODEL FR735
K Number
K070178
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Aesculap Implant System, Inc.
Date Received
January 19, 2007
Decision Date
April 30, 2007
Product Code
MAI
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
MAI Fastener, Fixation, Biodegradable, Soft Tissue

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K130887 S4C NAVIGATION INSTRUMENTS
K123909 AESCULAP CESPACE XP
K130291 S4 SPINAL SYSTEM
K122985 COLUMBUS REVISION KNEE SYSTEM
K112551 S4 SPINAL SYSTEM
K101281 VEGA KNEE SYSTEM
Search all 18 clearances from Aesculap Implant System, Inc. →