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

STRYKER PEEK AND TITANIUM SOFT EYELET ANCHORS

K Number: K071157 · Decision Sep 17, 2007
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
101
Review Days
145

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Basic Information

Device Name
STRYKER PEEK AND TITANIUM SOFT EYELET ANCHORS
K Number
K071157
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Endoscopy
Date Received
April 25, 2007
Decision Date
September 17, 2007
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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