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

SPEED ARC

K Number: K133270 · Decision Apr 17, 2014
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
230
Applicant Total
10
Review Days
176

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Basic Information

Device Name
SPEED ARC
K Number
K133270
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Biomedical Enterprises, Inc.
Date Received
October 23, 2013
Decision Date
April 17, 2014
Product Code
JDR
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
JDR Staple, Fixation, Bone

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Other Clearances by Biomedical Enterprises, Inc.

K Number Device Name
K153573 Converge
K150125 Elite Nitinol Fixation System
K143023 Nitinol Compression Plating System
K142292 Speed, Speed Shift, Speed Titan, Speed Arc
K133520 HAMMERLOCK 2
K124022 SPEED SHIFT
K061385 OSSTAPLE, OSSPLATE, OSSFORCE
K023486 OSSTAPLE, MAXILLOFACIAL
K023488 OSSTAPLE, CRANIOFACIAL