PEBA Anchor/Suture Combination, 2.0mm Mini-Tac Anchor, Model 10-1629-01, Modification to Twinfix Ti Quick-T, Twinfix FT PK, Twinfix Ultra Ti, Twinfix Ultra PK, Twinfix Ultra HA Suture Anchors, FOOTPRINT Ultra OK Suture Anchors, BIORAPTOR 2.9 Suture Anchor, BIORAPTOR 2.3 PK Suture Anchor, OSTEORAPTOR Suture Anchor, BIORAPTOR Knotless Suture Anchor, HEALICOIL PK Suture Anchor (formerly Next Generation Fully Threaded Suture Anchor), Bioraptor Curved 2.3 PK Suture Anchors
K152566 is the FDA 510(k) clearance record for PEBA Anchor/Suture Combination, 2.0mm Mini-Tac Anchor, Model 10-1629-01, Modification to Twinfix Ti Quick-T, Twinfix FT PK, Twinfix Ultra Ti, Twinfix Ultra PK, Twinfix Ultra HA Suture Anchors, FOOTPRINT Ultra OK Suture Anchors, BIORAPTOR 2.9 Suture Anchor, BIORAPTOR 2.3 PK Suture Anchor, OSTEORAPTOR Suture Anchor, BIORAPTOR Knotless Suture Anchor, HEALICOIL PK Suture Anchor (formerly Next Generation Fully Threaded Suture Anchor), Bioraptor Curved 2.3 PK Suture Anchors, a class II device, cleared for Smith & Nephew, Inc. on under FDA product code MBI (Fastener, Fixation, Nondegradable, Soft Tissue). FDA records list 572 510(k) clearances for Smith & Nephew, Inc., from to . As of , FDA records show 2 recalls naming K152566.
Clearance record
- Decision date
- Received
- (84 days to decision)
- Product code
- MBI Fastener, Fixation, Nondegradable, Soft Tissue
- Regulation
- 21 CFR 888.3040
- Device class
- Class II
- Review panel
- Orthopedic
- Applicant
- Smith & Nephew, Inc. 130 Forbes Blvd., Mansfield MA
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code MBI
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 1 |
| December 2025 | 2 |
| January 2026 | 3 |
| February 2026 | 1 |
| March 2026 | 9 |
| April 2026 | 1 |
| May 2026 | 4 |
| June 2026 | 1 |
| July 2026 | 4 |
| August 2026 | 2 |
| September 2026 | 3 |
| October 2026 | 0 |
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