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

TREACE DRILL SYSTEM

K Number: K862807 · Decision Aug 15, 1986
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
90
Applicant Total
80
Review Days
23

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Basic Information

Device Name
TREACE DRILL SYSTEM
K Number
K862807
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4250
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Treace Medical, Inc.
Date Received
July 23, 1986
Decision Date
August 15, 1986
Product Code
ERL
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece

Similar 510(k) Clearances

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

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Other Clearances by Treace Medical, Inc.

K Number Device Name
K883727 BUCKET PROSTHESIS PORP
K882349 MALLET, SURGICAL
K874779 BIPOLATOR 50
K873154 TREACE MAGNUM OTO-TOOL SYSTEM
K872000 EYE GARD
K870765 CANNULATED INSTRUMENT CLEANERS
K871706 OPTHA PREP
K870759 CLEANING SOLUTION, CATALOG NO. 8203
K870766 PROSTHESIS WIRE
K870760 BUR BRUSH
Search all 80 clearances from Treace Medical, Inc. →