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

ACUMED SUTURE ANCHOR

K Number: K993657 · Decision Jan 13, 2000
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
43
Review Days
77

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Basic Information

Device Name
ACUMED SUTURE ANCHOR
K Number
K993657
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Acu Med, Inc.
Date Received
October 28, 1999
Decision Date
January 13, 2000
Product Code
MBI
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
MBI Fastener, Fixation, Nondegradable, Soft Tissue

Similar 510(k) Clearances

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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
K980103 ACUMED SUTURE ANCHOR
K965028 ACUMED SUTURE WASHER
K965029 STABLELOC II EXTERNAL FIXATOR
K964500 ACUMED TENSION BAND PIN
K963026 TBD
K963118 EXTREMITY BONE SCREW
Search all 43 clearances from Acu Med, Inc. →