MEMOMETAL IMPLANTS (K-SNAP & TI-FUSE)— 510(k) K102072
Substantially EquivalentMemometal Technologies
FDA 510(k) clearance K102072 for MEMOMETAL IMPLANTS (K-SNAP & TI-FUSE), Substantially Equivalent on 2010-11-03. Applicant: Memometal Technologies. Device class: 2.
Clearance details
- Applicant
- Memometal Technologies
- Product code
- Code HTY
- Device class
- Class 2
- Regulation
- 21 CFR 888.3040
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bruz, FR
Recent devices under product code HTY
view allMore clearances from Memometal Technologies
view all- K112197 — MEMOMETAL INTRA-MEDULLARY BONE FASTENER
- K101930 — MEMOMETAL NAVIS BONE PLATING SYSTEM
- K093820 — SUBFIX ARTHROEREISIS IMPLANT, MODELS SUT0065, SUT0080, SUT0090, SUT0100, SUT0115
- K083447 — MEMOMETAL ANCHORAGE BONE PLATE SYSTEM, MODELS PLSS/PLSL, PLP10/PLP20/PLP30/PLP40/PLP50
- K071941 — MEMOMETAL BONE ANCHORS
Adverse events under product code HTY
product code HTY- Injury
- 544
- Total
- 544
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.