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

MODIFICATION TO HBS HEADLESS BONE SCREW

K Number: K101030 · Decision Jun 3, 2010
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
41
Review Days
51

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Basic Information

Device Name
MODIFICATION TO HBS HEADLESS BONE SCREW
K Number
K101030
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biopro, Inc.
Date Received
April 13, 2010
Decision Date
June 3, 2010
Product Code
HWC
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
HWC Screw, Fixation, Bone

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K121973 BIOPRO HEMI-EDGE TOE SYSTEM
K100761 BIOPRO POLAR HEAD
K090208 BIOPRO FEMORAL HEADS
K083490 BIOPRO K-WIRE, MODELS 16863, 17231, 17232, 18577, 18682-18685
K082705 BIOPRO BIPOLAR HEAD, MODELS 18130-18152
K081149 BIOPRO GO-EZ SCREW
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