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

Compressyn™ Staple

K Number: K171473 · Decision Nov 7, 2017
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
230
Applicant Total
10
Review Days
172

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Basic Information

Device Name
Compressyn™ Staple
K Number
K171473
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dallen Medical, Inc.
Date Received
May 19, 2017
Decision Date
November 7, 2017
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 Dallen Medical, Inc.

K Number Device Name
K150359 Tensyn Plug
K143092 Tensyn Plug
K141264 TENSYN BAND, TENSYN FRACTURE PLATES
K140358 COMPRESSYN STAPLE
K133858 TENSYN BAND
K132875 COMPRESSYN STAPLE
K131850 TENSYN BAND
K130431 COMPRESSYN BAND
K122871 COMPRESSYN STAPLE