ACTAEON PROBE— 510(k) K013429
Substantially EquivalentOsteobiologics, Inc.
FDA 510(k) clearance K013429 for ACTAEON PROBE, Substantially Equivalent on 2002-01-11. Applicant: Osteobiologics, Inc.. Device class: 2.
Clearance details
- Applicant
- Osteobiologics, Inc.
- Product code
- Code NGR
- Device class
- Class 2
- Regulation
- 21 CFR 888.1100
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Antonio, TX, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.