BIOBUCK CEMENT RESTRICTOR— 510(k) K023680
Substantially EquivalentSmith & Nephew, Inc.
FDA 510(k) clearance K023680 for BIOBUCK CEMENT RESTRICTOR, Substantially Equivalent on 2002-11-19. Applicant: Smith & Nephew, Inc.. Device class: 2.
Clearance details
- Applicant
- Smith & Nephew, Inc.
- Product code
- Code LZN
- Device class
- Class 2
- Regulation
- 21 CFR 878.3300
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Memphis, TN, US
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