SURGICAL DYNAMICS DISCOGRAPHY SYSTEM— 510(k) K921950

Unknown

Surgical Dynamics, Inc.

FDA 510(k) clearance K921950 for SURGICAL DYNAMICS DISCOGRAPHY SYSTEM, Unknown on 1993-06-07. Applicant: Surgical Dynamics, Inc.. Device class: 2.

Clearance details

Applicant
Surgical Dynamics, Inc.
Product code
Code FMI
Device class
Class 2
Regulation
21 CFR 880.5570
Advisory panel
General Hospital
Date received
Decision date
Decision
Unknown
Clearance type
Traditional
Location
Alameda, CA, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code FMI

product code FMI
Death
28
Injury
1,517
Malfunction
23,981
Other
18
Total
25,544

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 →

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