LINK, ACETABULAR REVISION MESH CUP— 510(k) K972760
Substantially EquivalentLink America, Inc.
FDA 510(k) clearance K972760 for LINK, ACETABULAR REVISION MESH CUP, Substantially Equivalent on 1997-10-22. Applicant: Link America, Inc.. Device class: 2.
Clearance details
- Applicant
- Link America, Inc.
- Product code
- Code JDJ
- Device class
- Class 2
- Regulation
- 21 CFR 878.3300
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Denville, NJ, US
Recent devices under product code JDJ
view allMore clearances from Link America, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.