HAPSET HYDROXYLAPATITE BONE GRAFT PLASTER— 510(k) K961511
Substantially EquivalentLifecore Biomedical, Inc.
FDA 510(k) clearance K961511 for HAPSET HYDROXYLAPATITE BONE GRAFT PLASTER, Substantially Equivalent on 1996-06-28. Applicant: Lifecore Biomedical, Inc.. Device class: 2.
Clearance details
- Applicant
- Lifecore Biomedical, Inc.
- Product code
- Code LZK
- Device class
- Class 2
- Regulation
- 21 CFR 878.3550
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Chaska, MN, US
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