510(k) · Cleared
ClearedQuadra-P
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Medacta International S.A. · LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Cleared on Jan 6, 2020 as substantially equivalent to K181254 (Medacta International S.A., 2018) and 1 other predicate after a 96-day review. Its family tree reaches back 10 generations to 1994. 6 later devices descend from it.
- Decided
- Jan 6, 2020
- Review
- 96 days
- Class
- Class II
- Product code
- LZO
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 10 generations to K935452 (1994). 76 ancestors in all, the oldest K845025 (1985). 6 later devices descend from it, 6 citing it directly.
- Root · 10 generations backK935452 P.F.C. 2 Total Hip System Porous Coated Modular Femoral ComponentJohnson & Johnson Orthopaedics, Inc. · 1994
- 6 generations between
- 3 generations backK161635 AMIStem-H Proximal CoatingMedacta International S.A. · 2017
- 2 generations backK173794 AMIStem-H Proximal Coating, AMIStem-P and AMIStem-P CollaredMedacta International S.A. · 2018
- 1 generation backK181254 Quadra PMedacta International S.A. · 2018
- This deviceK192827 Quadra-PMedacta International S.A. · 2020
- Descendant · cites it directly · 1 of its ownK202730 Quadra-PMedacta International S.A. · 2020
- Descendant · cites it directly · 1 of its ownK203041 SMS Cementless StemMedacta International S.A. · 2020
- Descendant · cites it directly · 0 of its ownK250450 Coated hip implantsMedacta International S.A. · 2025
- Descendant · cites it directly · 0 of its ownK251166 Mfinity Femoral SystemMedacta International S.A. · 2025
- Descendant · cites it directly · 0 of its ownK220405 Amis K LongMedacta International S.A. · 2022
Show all 10 generations
- Root · 10 generations backK935452 P.F.C. 2 Total Hip System Porous Coated Modular Femoral ComponentJohnson & Johnson Orthopaedics, Inc. · 1994
- 9 generations backK945518 P.F.C. 2 Total Hip System Porous Coated Modular Femoral ComponentJohnson & Johnson Professionals, Inc. · 1996
- 8 generations backK961939 S-Rom Femoral Hip Stem (Sizes 12 X 06 X 115 and 12 X 07 X 115)Johnson & Johnson Professionals, Inc. · 1996
- 7 generations backK974331 Uni-Rom Total Hip System Femoral StemJohnson & Johnson Professionals, Inc. · 1998
- 6 generations backK001991 Titan Porocoat Hip ProsthesisDePuy Orthopaedics, Inc. · 2000
- 5 generations backK042992 Corail Amt Hip ProsthesisDePuy Orthopaedics, Inc. · 2005 · Recalled
- 4 generations backK123392 Avenir Muller StemZimmer GmbH · 2013 · Recalled
- 3 generations backK161635 AMIStem-H Proximal CoatingMedacta International S.A. · 2017
- 2 generations backK173794 AMIStem-H Proximal Coating, AMIStem-P and AMIStem-P CollaredMedacta International S.A. · 2018
- 1 generation backK181254 Quadra PMedacta International S.A. · 2018
- This deviceK192827 Quadra-PMedacta International S.A. · 2020
Showing 5 of 6 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 6 · See all- K202730Quadra-PMedacta International S.A. · 2020 · cites it directly1descendant
- K203041SMS Cementless StemMedacta International S.A. · 2020 · cites it directly1descendant
- K250450Coated hip implantsMedacta International S.A. · 2025 · cites it directly0descendants
- K251166Mfinity Femoral SystemMedacta International S.A. · 2025 · cites it directly0descendants
- K220405Amis K LongMedacta International S.A. · 2022 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −10 | K935452 | P.F.C. 2 Total Hip System Porous Coated Modular Femoral Component | Johnson & Johnson Orthopaedics, Inc. | 1994 | — |
| −9 | K945518 | P.F.C. 2 Total Hip System Porous Coated Modular Femoral Component | Johnson & Johnson Professionals, Inc. | 1996 | — |
| −8 | K961939 | S-Rom Femoral Hip Stem (Sizes 12 X 06 X 115 and 12 X 07 X 115) | Johnson & Johnson Professionals, Inc. | 1996 | — |
| −7 | K974331 | Uni-Rom Total Hip System Femoral Stem | Johnson & Johnson Professionals, Inc. | 1998 | — |
| −6 | K001991 | Titan Porocoat Hip Prosthesis | DePuy Orthopaedics, Inc. | 2000 | — |
| −5 | K042992 | Corail Amt Hip Prosthesis | DePuy Orthopaedics, Inc. | 2005 | 1 |
| −4 | K123392 | Avenir Muller Stem | Zimmer GmbH | 2013 | 4 |
| −3 | K161635 | AMIStem-H Proximal Coating | Medacta International S.A. | 2017 | — |
| −2 | K173794 | AMIStem-H Proximal Coating, AMIStem-P and AMIStem-P Collared | Medacta International S.A. | 2018 | — |
| −1 | K181254 | Quadra P | Medacta International S.A. | 2018 | — |
| 0 (this device) | K192827 | Quadra-P | Medacta International S.A. | 2020 | — |
| +1 | K202730 | Quadra-P | Medacta International S.A. | 2020 | — |
| +1 | K203041 | SMS Cementless Stem | Medacta International S.A. | 2020 | — |
| +1 | K250450 | Coated hip implants | Medacta International S.A. | 2025 | — |
| +1 | K251166 | Mfinity Femoral System | Medacta International S.A. | 2025 | — |
| +1 | K220405 | Amis K Long | Medacta International S.A. | 2022 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1985 | 3 | 0 |
| 1987 | 2 | 0 |
| 1988 | 2 | 0 |
| 1990 | 1 | 0 |
| 1991 | 2 | 0 |
| 1992 | 2 | 0 |
| 1993 | 1 | 0 |
| 1994 | 8 | 0 |
| 1995 | 2 | 0 |
| 1996 | 8 | 0 |
| 1997 | 2 | 0 |
| 1998 | 2 | 0 |
| 1999 | 4 | 0 |
| 2000 | 7 | 0 |
| 2001 | 2 | 0 |
| 2002 | 4 | 0 |
| 2003 | 3 | 0 |
| 2004 | 2 | 0 |
| 2005 | 1 | 0 |
| 2006 | 1 | 0 |
| 2007 | 1 | 0 |
| 2008 | 3 | 0 |
| 2009 | 1 | 0 |
| 2010 | 1 | 0 |
| 2012 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2020 | 2 | 0 |
| 2021 | 1 | 0 |
| 2022 | 1 | 0 |
| 2025 | 2 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in LZO? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new LZO device
- #1 K251292 RECLAIM Monobloc Revision Femoral Stemscore 17.8 · 19 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K181254 | Quadra PSummary page 4…0, 21 CFR 888.3358, Device Classification 11 III. Predicate Device Substantial equivalence is claimed to the following devices: Primary predicate device: e Quadra-P, K181254, Medacta International SA Secondary predicate device: e Medacta Total Hip Prosthesis System — Quadra C (also referred to as “Qua… | 2018 |
| * | K083558 | Medacta Total Hip Prosthesis System - Quadra CSummary page 4…ate device: e Quadra-P, K181254, Medacta International SA Secondary predicate device: e Medacta Total Hip Prosthesis System — Quadra C (also referred to as “Quadra C”), K083558, Medacta International SA The following devices are referenced: e AMIStem-H Proximal Coating, K121011, Medacta International SA… | 2009 |
| † | K121011 | Amistem and Quadra - Line Extension | 2012 |
| † | K173794 | AMIStem-H Proximal Coating, AMIStem-P and AMIStem-P Collared | 2018 |
What descends from it? (6)
6 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 26 years and passes through 5 companies; a new generation was cleared every 1.5 years on median.
- 19 of the 76 ancestors have a recall of any class.
- Of its descendants, K202730 (Medacta International S.A., 2020) has gone furthest, with 1 descendant of its own.
- 3 other devices also cite its predicate K181254.
How does its category compare?
All LZO devicesLZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.
FDA decisions per year · LZO
14in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · LZO
119in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LZO
1in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · LZO
3,244in 2025
MAUDE reports naming product code LZO, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 9 | 87 | 2 | 138 |
| 2008 | 11 | 63 | 13 | 125 |
| 2009 | 7 | 83 | 42 | 189 |
| 2010 | 15 | 78 | 0 | 394 |
| 2011 | 13 | 87 | 10 | 544 |
| 2012 | 14 | 98 | 14 | 963 |
| 2013 | 26 | 100 | 0 | 1,370 |
| 2014 | 13 | 85 | 1 | 1,477 |
| 2015 | 12 | 115 | 1 | 1,348 |
| 2016 | 10 | 177 | 9 | 1,728 |
| 2017 | 16 | 257 | 5 | 2,165 |
| 2018 | 18 | 163 | 2 | 3,133 |
| 2019 | 28 | 109 | 4 | 3,066 |
| 2020 | 18 | 112 | 3 | 1,963 |
| 2021 | 12 | 170 | 0 | 2,199 |
| 2022 | 11 | 279 | 4 | 1,985 |
| 2023 | 10 | 122 | 2 | 2,066 |
| 2024 | 11 | 111 | 1 | 2,586 |
| 2025 | 14 | 119 | 1 | 3,244 |
| 2026 | 9 | 102 | 0 | — |
What is it indicated for?
The hip prostheses QUADRA-P and QUADRA-P collared are designed for cementless use in total or partial hip arthroplasty, for primary or revision surgery. The hip prosthesis QUADRA-P cemented is designed for cemented use in total or partial hip arthroplasty in primary or revision surgery. Hip replacement is indicated in the following cases: * Severely painful and/or disabled joint as a result of arthrosis, traumatic arthritis, rheumatoid polyarthritis or…
Read the full statement (109 words)
The hip prostheses QUADRA-P and QUADRA-P collared are designed for cementless use in total or partial hip arthroplasty, for primary or revision surgery. The hip prosthesis QUADRA-P cemented is designed for cemented use in total or partial hip arthroplasty in primary or revision surgery. Hip replacement is indicated in the following cases:
* Severely painful and/or disabled joint as a result of arthrosis, traumatic arthritis, rheumatoid polyarthritis or congenital hip dysplasia
* Avascular necrosis of the femoral head
* Acute traumatic fracture of the femoral head or neck
* Failure of previous hip surgery: joint reconstruction, internal fixation, arthrodesis, partial hip arthroplasty, hip resurfacing replacement or total hip arthroplasty.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K192827 · printed Nov 6, 2026
Cite this page
510(k) Report. “K192827: Quadra-P.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K192827
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026