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

OSTEOTECH NAVICULAR AND CANCELLOUS CANNULATED SCREWS

K Number: K950652 · Decision Jun 22, 1995
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
24
Review Days
129

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Basic Information

Device Name
OSTEOTECH NAVICULAR AND CANCELLOUS CANNULATED SCREWS
K Number
K950652
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Osteotech, Inc.
Date Received
February 13, 1995
Decision Date
June 22, 1995
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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Other Clearances by Osteotech, Inc.

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K081227 PLEXUR M
K080511 PLEXUR-P
K073405 PLEXUR M
K061982 PLEXUR P
K051188 GRAFTON DBM
K051781 GRAFTCAGE TLX
K051195 GRAFTON DBM
K043209 VIAGRAF DBM PASTE
K053080 GRAFTCAGE ACX
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