510(k) · Cleared
ClearedCorin Metafix Hip Stem
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Corin USA · LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Cleared on May 24, 2013 as substantially equivalent to K082525 (Corin USA, 2010) and 3 other predicates after a 74-day review. Its family tree reaches back 14 generations to 1981. 5 later devices descend from it.
- Decided
- May 24, 2013
- Review
- 74 days
- Class
- Class II
- Product code
- LZO
- Recalls
- None
- Predicates
- 4
Its longest line of descent runs back 14 generations to K810258 (1981). 121 ancestors in all. 5 later devices descend from it, 2 citing it directly.
- Root · 14 generations backK810258 Proximal Fermoral Hip ReplacementBiomet, Inc. · 1981
- 10 generations between
- 3 generations backK111911 Corin Optimom Modular HeadCorin USA · 2011
- 2 generations backK120362 Metafix Femoral Stem for Hemi-ArthroplastyCorin USA · 2012
- 1 generation backK121439 Metafix Femoral Hip Stem Size 1Corin USA · 2012
- This deviceK130634 Corin Metafix Hip StemCorin USA · 2013
- Descendant · cites it directly · 4 of its ownK131952 Corin Metafix Hip StemCorin USA · 2013
- Descendant · cites it directly · 3 of its ownK162942 Corin MetaFix Hip StemCorin U.S.A. Limited · 2017
- Descendant · 2 generations on · 2 of its ownK212069 Corin MetaFix™ Hip StemCorin U.S.A. Limited · 2022
- Descendant · 3 generations on · 1 of its ownK241472 Icona Hip StemCorin U.S.A. Limited · 2024
- Descendant · 4 generations on · 0 of its ownK261576 Icona Hip StemCorin, Ltd. · 2026
Show all 14 generations
- Root · 14 generations backK810258 Proximal Fermoral Hip ReplacementBiomet, Inc. · 1981
- 13 generations backK974558 Salvage/Onocology Hip and Total Femur SystemBiomet, Inc. · 1998
- 12 generations backK032396 Ringloc 36MM Line and Modular Femoral HeadsBiomet, Inc. · 2003 · Recalled
- 11 generations backK042051 Arcomxl Polyethylene LinersBiomet, Inc. · 2005 · Recalled
- 10 generations backK051411 Arcomxl Polyethylene Liners and Biolox Delta HeadsBiomet, Inc. · 2005 · Recalled
- 9 generations backK061312 36MM Biolox Delta Ceramic HeadsBiomet, Inc. · 2006
- 8 generations backK071535 Biolox Delta Ceramic Femoral HeadZimmer, Inc. · 2007 · Recalled
- 7 generations backK082844 Biolox Delta Ceramic Femoral Head, Biolox Delta Ceramic Femoral Head…Encore Medical L.P. · 2008 · Recalled
- 6 generations backK100412 Biolox Delta Ceramic Femoral HeadsSmith & Nephew, Inc. · 2010
- 5 generations backK103120 Corin Biolox Delta Femoral HeadsCorin USA · 2011
- 4 generations backK110087 Corin Trinity Acetbular System with Hxlpe LinersCorin USA · 2011
- 3 generations backK111911 Corin Optimom Modular HeadCorin USA · 2011
- 2 generations backK120362 Metafix Femoral Stem for Hemi-ArthroplastyCorin USA · 2012
- 1 generation backK121439 Metafix Femoral Hip Stem Size 1Corin USA · 2012
- This deviceK130634 Corin Metafix Hip StemCorin USA · 2013
Most influential descendants
Showing 5 of 5 · See all- K131952Corin Metafix Hip StemCorin USA · 2013 · cites it directly4descendants
- K162942Corin MetaFix Hip StemCorin U.S.A. Limited · 2017 · cites it directly3descendants
- K212069Corin MetaFix™ Hip StemCorin U.S.A. Limited · 2022 · 2 generations on2descendants
- K241472Icona Hip StemCorin U.S.A. Limited · 2024 · 3 generations on1descendant
- K261576Icona Hip StemCorin, Ltd. · 2026 · 4 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −14 | K810258 | Proximal Fermoral Hip Replacement | Biomet, Inc. | 1981 | — |
| −13 | K974558 | Salvage/Onocology Hip and Total Femur System | Biomet, Inc. | 1998 | — |
| −12 | K032396 | Ringloc 36MM Line and Modular Femoral Heads | Biomet, Inc. | 2003 | 3 |
| −11 | K042051 | Arcomxl Polyethylene Liners | Biomet, Inc. | 2005 | 1 |
| −10 | K051411 | Arcomxl Polyethylene Liners and Biolox Delta Heads | Biomet, Inc. | 2005 | 1 |
| −9 | K061312 | 36MM Biolox Delta Ceramic Heads | Biomet, Inc. | 2006 | — |
| −8 | K071535 | Biolox Delta Ceramic Femoral Head | Zimmer, Inc. | 2007 | 3 |
| −7 | K082844 | Biolox Delta Ceramic Femoral Head, Biolox Delta Ceramic Femoral Head Offset… | Encore Medical L.P. | 2008 | 1 |
| −6 | K100412 | Biolox Delta Ceramic Femoral Heads | Smith & Nephew, Inc. | 2010 | — |
| −5 | K103120 | Corin Biolox Delta Femoral Heads | Corin USA | 2011 | — |
| −4 | K110087 | Corin Trinity Acetbular System with Hxlpe Liners | Corin USA | 2011 | — |
| −3 | K111911 | Corin Optimom Modular Head | Corin USA | 2011 | — |
| −2 | K120362 | Metafix Femoral Stem for Hemi-Arthroplasty | Corin USA | 2012 | — |
| −1 | K121439 | Metafix Femoral Hip Stem Size 1 | Corin USA | 2012 | — |
| 0 (this device) | K130634 | Corin Metafix Hip Stem | Corin USA | 2013 | — |
| +1 | K131952 | Corin Metafix Hip Stem | Corin USA | 2013 | — |
| +1 | K162942 | Corin MetaFix Hip Stem | Corin U.S.A. Limited | 2017 | — |
| +2 | K212069 | Corin MetaFix™ Hip Stem | Corin U.S.A. Limited | 2022 | — |
| +3 | K241472 | Icona Hip Stem | Corin U.S.A. Limited | 2024 | — |
| +4 | K261576 | Icona Hip Stem | Corin, Ltd. | 2026 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1984 | 1 | 0 |
| 1985 | 2 | 0 |
| 1987 | 1 | 0 |
| 1990 | 1 | 0 |
| 1991 | 4 | 0 |
| 1992 | 4 | 0 |
| 1993 | 4 | 0 |
| 1994 | 15 | 0 |
| 1995 | 6 | 0 |
| 1996 | 9 | 0 |
| 1997 | 6 | 0 |
| 1998 | 4 | 0 |
| 1999 | 5 | 0 |
| 2000 | 12 | 0 |
| 2001 | 6 | 0 |
| 2002 | 8 | 0 |
| 2003 | 3 | 0 |
| 2004 | 6 | 0 |
| 2005 | 3 | 0 |
| 2006 | 1 | 0 |
| 2007 | 1 | 0 |
| 2009 | 2 | 0 |
| 2010 | 2 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2013 | 1 | 0 |
| 2017 | 1 | 0 |
| 2022 | 1 | 0 |
| 2024 | 1 | 0 |
| 2026 | 1 | 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 K192827 Quadra-Pscore 19.3 · 10 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (4)
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 |
|---|---|---|---|
| * | K082525 | Corin Metafix Femoral StemSummary page 2…or effective use. The indications and compatible components for use with the Corin Metafix stem subject of this submission are identical to that of the predicate devices K082525, K120362 & 1(121439. 10. Intended Use / Indications: The indications for the Corin Metafix Flip Stern as a total hip arthroplas… | 2010 |
| * | K120362 | Metafix Femoral Stem for Hemi-ArthroplastySummary page 2…ive use. The indications and compatible components for use with the Corin Metafix stem subject of this submission are identical to that of the predicate devices K082525, K120362 & 1(121439. 10. Intended Use / Indications: The indications for the Corin Metafix Flip Stern as a total hip arthroplasty and, w… | 2012 |
| * | K121439 | Metafix Femoral Hip Stem Size 1Summary page 2…ed: * tuorin Mfetafix Flip Stem (1(082525) * Corin Metafix Femoral Stern for Hleri-Arthroplasty (1(120362) a Corin Mletafix H-ip Stem (1K121 439) a DePuv Orthopaedics Corail AMNT Hip Systetm (K(042992) 9. Device Description: The Corin M~etafix Hip Stem is a… | 2012 |
| * | K042992 | Corail Amt Hip ProsthesisSummary page 3…/indications for use, design, materials and sizes and similar in terms of contraindications. it is similar to the predicate Deipuy Orthopaedics Corail AMT F-lip System (1K042992) in terms of intended Luse/indications for use, contraindlications, and is identical in terms of material and coating. Based on t… | 2005 |
What descends from it? (5)
2 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 32 years and passes through 5 companies; a new generation was cleared every 11 months on median.
- 28 of the 120 ancestors have a recall of any class.
- Of its descendants, K131952 (Corin USA, 2013) has gone furthest, with 4 descendants of its own.
- 9 other devices also cite its predicate K082525.
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. 2013, 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 indications for the Corin Metafix Hip Stem as a total hip arthroplasty and, when used in
combination with Corin hemi-arthroplasty femoral heads, as a hemiarthroplasty, include:
Non-inflammatory degenerative joint disease including osteoarthritis and avascular
necrosis
Rheumatoid arthritis
Correction of functional deformity
Treatment of non-union, femoral neck and trochanteric fractures of the proximal femur
Developmental dysplasia of the hip (DDH) and congenital dysplasia of the hip (CDH)
The Corin Metafix Hip Stem is indicated for cementless use only.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K130634 · printed Nov 6, 2026
Cite this page
510(k) Report. “K130634: Corin Metafix Hip Stem.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K130634
Report an extraction error
Are you the manufacturer?
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