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

BONE ANCHOR FOR SOFT TISSUE ATTACHMENT

K Number: K932925 · Decision Apr 26, 1994
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
230
Applicant Total
3
Review Days
315

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Basic Information

Device Name
BONE ANCHOR FOR SOFT TISSUE ATTACHMENT
K Number
K932925
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vesitec Medical, Inc.
Date Received
June 15, 1993
Decision Date
April 26, 1994
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

Similar 510(k) Clearances

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Other Clearances by Vesitec Medical, Inc.

K Number Device Name
K931182 VESITEC DRILL GUIDE
K931181 VESITEC SUTURE PASSER