BIOASBSORBABLE MINI-SCREW SUTURE ANCHOR— 510(k) K960555

Name: FDA 510(k) clearance K960555
Creator: U.S. Food and Drug Administration
Published: 1996-07-09

Substantially Equivalent

Instrument Makar, Inc.

FDA 510(k) clearance K960555 for BIOASBSORBABLE MINI-SCREW SUTURE ANCHOR, Substantially Equivalent on 1996-07-09. Applicant: Instrument Makar, Inc.. Device class: 2.

Clearance details

Applicant: Instrument Makar, Inc.
Product code: Code MAI
Device class: Class 2
Regulation: 21 CFR 888.3030
Advisory panel: Orthopedic
Date received: 1996-02-09
Decision date: 1996-07-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lansing, MI, US

Download summary PDF View on FDA.gov ↗

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K963396 — BIOSPHERE SUTURE ANCHOR1997-05-06
K964364 — DISPOSABLE APRON1997-02-25
K955835 — FLUID BARRIER BOOT KNEE & ANKLE-HIGH1996-11-19

Adverse events under product code MAI

product code MAI

Injury: 1,948
Malfunction: 8,580
Total: 10,528

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.