Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue Technology— 510(k) K170456
Substantially EquivalentStryker Sustainability Solutions
FDA 510(k) clearance K170456 for Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue Technology, Substantially Equivalent on 2017-04-05. Applicant: Stryker Sustainability Solutions. Device class: Unclassified.
Clearance details
- Applicant
- Stryker Sustainability Solutions
- Product code
- Code NLQ
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tempe, AZ, US
Recent devices under product code NLQ
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- K233471 — Reprocessed HARMONIC 1100 Shears, 5mm Diameter, 20cm length (HAR1120) +1 more
- K202554 — Reprocessed HARMONIC ACE+ 7, 5 mm Diameter Shears with Advanced Hemostasis
- K193563 — Medline ReNewal Reprocessed Harmonic ACE+7 Shears
More clearances from Stryker Sustainability Solutions
view all- K260636 — Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coating
- K241758 — Reprocessed RD SET Adt Pulse Oximeter Sensor (4000) +3 more
- K231621 — Reprocessed ViewFlex Xtra ICE Catheter (D087031)
- K230251 — Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)
- K230255 — Remanufactured LigaSure Exact Dissector Without Nano-coating LF2019
Recalls naming K170456
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K170456.
Data sourced from openFDA. This site is unofficial and independent of the FDA.