FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ACUMED BONE GRAFT SYSTEM

K Number: K960711 · Decision May 7, 1996
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
28
Applicant Total
43
Review Days
76

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Basic Information

Device Name
ACUMED BONE GRAFT SYSTEM
K Number
K960711
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Acu Med, Inc.
Date Received
February 21, 1996
Decision Date
May 7, 1996
Product Code
KIJ
Advisory Committee
General, Plastic Surgery
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
KIJ Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KIJ), ordered by most recent decision date.

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Other Clearances by Acu Med, Inc.

K Number Device Name
K021321 WRIST FUSION PLATE
K013616 POLARUS CAP SCREW
K012655 CONGRUENT BONE PLATE SYSTEM
K992525 ACUMED MODULAR SHOULDER SYSTEM
K993657 ACUMED SUTURE ANCHOR
K980103 ACUMED SUTURE ANCHOR
K965028 ACUMED SUTURE WASHER
K965029 STABLELOC II EXTERNAL FIXATOR
K964500 ACUMED TENSION BAND PIN
K963026 TBD
Search all 43 clearances from Acu Med, Inc. →