OMNIFIT SELF TAPPING CANCELLOUS BONE SCREWS— 510(k) K894124

Substantially Equivalent for Some Indications

Osteonics Corp.

FDA 510(k) clearance K894124 for OMNIFIT SELF TAPPING CANCELLOUS BONE SCREWS, Substantially Equivalent for Some Indications on 1989-09-11. Applicant: Osteonics Corp.. Device class: 2.

Clearance details

Applicant
Osteonics Corp.
Product code
Code HWC
Device class
Class 2
Regulation
21 CFR 888.3040
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent for Some Indications
Clearance type
Traditional
Location
Allendale, NJ, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code HWC

product code HWC
Death
20
Injury
15,910
Malfunction
8,192
Other
1
Total
24,123

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

Recalls naming K894124

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K894124.

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