SYNTHES (USA) UNIV. SCREW FIXATION SYSTEM (TITANIUM)— 510(k) K951794
Substantially Equivalent for Some IndicationsSynthes (Usa)
FDA 510(k) clearance K951794 for SYNTHES (USA) UNIV. SCREW FIXATION SYSTEM (TITANIUM), Substantially Equivalent for Some Indications on 1995-08-21. Applicant: Synthes (Usa). Device class: 2.
Clearance details
- Applicant
- Synthes (Usa)
- Product code
- Code MNH
- Device class
- Class 2
- Regulation
- 21 CFR 888.3070
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent for Some Indications
- Clearance type
- Traditional
- Location
- Paoli, PA, US
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Adverse events under product code MNH
product code MNH- Injury
- 978
- Malfunction
- 793
- Total
- 1,771
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.